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 |
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