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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

✍ Scribed by T Freilinger; M Bohe; B Wegener; B Müller-Myhsok; M Dichgans; H Knoblauch

Book ID: 111092803
Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 82 KB
Volume: 28
Category: Article
ISSN: 0333-1024
DOI: 10.1111/j.1468-2982.2008.01540.x

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