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

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

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

T Freilinger,M Bohe,B Wegener,B ,M Dichgans,H Knoblauch,

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

T Freilinger,M Bohe,B Wegener,B ,M Dichgans,H Knoblauch,

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

PUBLICATION TYPE: Journal Article

Journal: Cephalalgia : an international journal of headache

VOLUME: 28

Page Numbers: 403-7

Journal Abbreviation: Cephalalgia

ISSN: 1468-2982

DAY: 14

MONTH: 02

YEAR: 2008

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

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LANGUAGE: eng

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AFFILIATION: Department of Neurology, Ludwig-Maximilians-Universität München, Klinikum Grosshadern, Munich, Germany. tobias.freilinger@med.uni-muenchen.de

Country: England

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MEDLINETA: Cephalalgia

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