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Analysis of the alpha-synuclein G209A mutation in familial Parkinson's disease.

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Title: Analysis of the alpha-synuclein G209A mutation in familial Parkinson's disease.
Authors: Zareparsi, Sepideh, Kay, Jeffrey, Camicioli, Richard, Kramer, Patricia, Nutt, John, Bird, Thomas, Litt, Michael, Payami, Haydeh, Zareparsi, S (AUTHOR), Kaye, J (AUTHOR), Camicioli, R (AUTHOR), Kramer, P (AUTHOR), Nutt, J (AUTHOR), Bird, T (AUTHOR), Litt, M (AUTHOR), Payami, H (AUTHOR), Kay, J (AUTHOR)
Source: Lancet. 1/3/1998, Vol. 351 Issue 9095, p37-38. 2p.
Subjects: Parkinson's disease & genetics, Brain diseases, Genetics, Age factors in disease, Comparative studies, Genealogy, Genetic techniques, Research methodology, Medical cooperation, Genetic mutation, Nerve tissue proteins, Parkinson's disease, Research, Evaluation research
Abstract: Presents research which sought to test whether a mutation in the alpha-synuclein gene on chromosome 4q21-23 is responsible for Parkinson's disease (PD) in white PD families of northern European origin. Previous research; None of subjects having mutation at G209A position; Linkage analysis; No positive evidence for linkage in most families; Alpha-synuclein not responsible for PD in these families.
Database: Psychology and Behavioral Sciences Collection
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Header DbId: pbh
DbLabel: Psychology and Behavioral Sciences Collection
An: 28781
AccessLevel: 6
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
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  Label: Title
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  Data: Analysis of the alpha-synuclein G209A mutation in familial Parkinson's disease.
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  Data: <searchLink fieldCode="AR" term="%22Zareparsi%2C+Sepideh%22">Zareparsi, Sepideh</searchLink><br /><searchLink fieldCode="AR" term="%22Kay%2C+Jeffrey%22">Kay, Jeffrey</searchLink><br /><searchLink fieldCode="AR" term="%22Camicioli%2C+Richard%22">Camicioli, Richard</searchLink><br /><searchLink fieldCode="AR" term="%22Kramer%2C+Patricia%22">Kramer, Patricia</searchLink><br /><searchLink fieldCode="AR" term="%22Nutt%2C+John%22">Nutt, John</searchLink><br /><searchLink fieldCode="AR" term="%22Bird%2C+Thomas%22">Bird, Thomas</searchLink><br /><searchLink fieldCode="AR" term="%22Litt%2C+Michael%22">Litt, Michael</searchLink><br /><searchLink fieldCode="AR" term="%22Payami%2C+Haydeh%22">Payami, Haydeh</searchLink><br /><searchLink fieldCode="AR" term="%22Zareparsi%2C+S%22">Zareparsi, S</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kaye%2C+J%22">Kaye, J</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Camicioli%2C+R%22">Camicioli, R</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kramer%2C+P%22">Kramer, P</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Nutt%2C+J%22">Nutt, J</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Bird%2C+T%22">Bird, T</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Litt%2C+M%22">Litt, M</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Payami%2C+H%22">Payami, H</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kay%2C+J%22">Kay, J</searchLink> (AUTHOR)
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  Data: <searchLink fieldCode="JN" term="%22Lancet%22">Lancet</searchLink>. 1/3/1998, Vol. 351 Issue 9095, p37-38. 2p.
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  Data: <searchLink fieldCode="DE" term="%22Parkinson's+disease+%26+genetics%22">Parkinson's disease & genetics</searchLink><br /><searchLink fieldCode="DE" term="%22Brain+diseases%22">Brain diseases</searchLink><br /><searchLink fieldCode="DE" term="%22Genetics%22">Genetics</searchLink><br /><searchLink fieldCode="DE" term="%22Age+factors+in+disease%22">Age factors in disease</searchLink><br /><searchLink fieldCode="DE" term="%22Comparative+studies%22">Comparative studies</searchLink><br /><searchLink fieldCode="DE" term="%22Genealogy%22">Genealogy</searchLink><br /><searchLink fieldCode="DE" term="%22Genetic+techniques%22">Genetic techniques</searchLink><br /><searchLink fieldCode="DE" term="%22Research+methodology%22">Research methodology</searchLink><br /><searchLink fieldCode="DE" term="%22Medical+cooperation%22">Medical cooperation</searchLink><br /><searchLink fieldCode="DE" term="%22Genetic+mutation%22">Genetic mutation</searchLink><br /><searchLink fieldCode="DE" term="%22Nerve+tissue+proteins%22">Nerve tissue proteins</searchLink><br /><searchLink fieldCode="DE" term="%22Parkinson's+disease%22">Parkinson's disease</searchLink><br /><searchLink fieldCode="DE" term="%22Research%22">Research</searchLink><br /><searchLink fieldCode="DE" term="%22Evaluation+research%22">Evaluation research</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: Presents research which sought to test whether a mutation in the alpha-synuclein gene on chromosome 4q21-23 is responsible for Parkinson's disease (PD) in white PD families of northern European origin. Previous research; None of subjects having mutation at G209A position; Linkage analysis; No positive evidence for linkage in most families; Alpha-synuclein not responsible for PD in these families.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=pbh&AN=28781
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1016/S0140-6736(05)78089-2
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      – Code: eng
        Text: English
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        PageCount: 2
        StartPage: 37
    Subjects:
      – SubjectFull: Parkinson's disease & genetics
        Type: general
      – SubjectFull: Brain diseases
        Type: general
      – SubjectFull: Genetics
        Type: general
      – SubjectFull: Age factors in disease
        Type: general
      – SubjectFull: Comparative studies
        Type: general
      – SubjectFull: Genealogy
        Type: general
      – SubjectFull: Genetic techniques
        Type: general
      – SubjectFull: Research methodology
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      – SubjectFull: Medical cooperation
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      – SubjectFull: Genetic mutation
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      – SubjectFull: Nerve tissue proteins
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      – SubjectFull: Parkinson's disease
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      – SubjectFull: Research
        Type: general
      – SubjectFull: Evaluation research
        Type: general
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      – TitleFull: Analysis of the alpha-synuclein G209A mutation in familial Parkinson's disease.
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              Text: 1/3/1998
              Type: published
              Y: 1998
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              Value: 351
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              Value: 9095
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