Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.
| Autor: | 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 |
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| Zdroj: | Cephalalgia. Apr2008, Vol. 28 Issue 4, p403-407. 5p. 1 Diagram, 2 Charts. |
| Databáze: | Academic Search Ultimate |
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