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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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.
ISSN:01406736
DOI:10.1016/S0140-6736(05)78089-2