Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.

Saved in:
Bibliographic Details
Title: Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.
Authors: Freilinger, T.1 tobias.freilinger@med.uni-muenchen.de, Bohe, M.1, Wegener, B.2, Müller-Myhsok, B.3, Dichgans, M.1, Knoblauch, H.2
Source: Cephalalgia. Apr2008, Vol. 28 Issue 4, p403-407. 5p. 1 Diagram, 2 Charts.
Database: Academic Search Ultimate
FullText Links:
  – Type: pdflink
Text:
  Availability: 0
Header DbId: asn
DbLabel: Academic Search Ultimate
An: 31147667
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Freilinger%2C+T%2E%22">Freilinger, T.</searchLink><relatesTo>1</relatesTo><i> tobias.freilinger@med.uni-muenchen.de</i><br /><searchLink fieldCode="AR" term="%22Bohe%2C+M%2E%22">Bohe, M.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Wegener%2C+B%2E%22">Wegener, B.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Müller-Myhsok%2C+B%2E%22">Müller-Myhsok, B.</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Dichgans%2C+M%2E%22">Dichgans, M.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Knoblauch%2C+H%2E%22">Knoblauch, H.</searchLink><relatesTo>2</relatesTo>
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22Cephalalgia%22">Cephalalgia</searchLink>. Apr2008, Vol. 28 Issue 4, p403-407. 5p. 1 Diagram, 2 Charts.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=31147667
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1111/j.1468-2982.2008.01540.x
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 5
        StartPage: 403
    Titles:
      – TitleFull: Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Freilinger, T.
      – PersonEntity:
          Name:
            NameFull: Bohe, M.
      – PersonEntity:
          Name:
            NameFull: Wegener, B.
      – PersonEntity:
          Name:
            NameFull: Müller-Myhsok, B.
      – PersonEntity:
          Name:
            NameFull: Dichgans, M.
      – PersonEntity:
          Name:
            NameFull: Knoblauch, H.
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 04
              Text: Apr2008
              Type: published
              Y: 2008
          Identifiers:
            – Type: issn-print
              Value: 03331024
          Numbering:
            – Type: volume
              Value: 28
            – Type: issue
              Value: 4
          Titles:
            – TitleFull: Cephalalgia
              Type: main
ResultId 1