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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
Authors: Freilinger, T.; Bohe, M.; Wegener, B.; Müller-Myhsok, B.; Dichgans, M.; Knoblauch, H.
Date of Publication (YYYY-MM-DD): 2008-04
Title of Journal: Cephalalgia
Volume: 28
Issue / Number: 4
Start Page: 403
End Page: 407
Document Type: Article
ID: 359306.0