Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.
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| Title: | Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation. |
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| Authors: | 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 |
| Source: | Cephalalgia. Apr2008, Vol. 28 Issue 4, p403-407. 5p. 1 Diagram, 2 Charts. |
| Database: | Academic Search Ultimate |
| ISSN: | 03331024 |
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| DOI: | 10.1111/j.1468-2982.2008.01540.x |
