Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation. (Q51893783)
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scientific article published on 14 February 2008
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English | Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation. |
scientific article published on 14 February 2008 |
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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. (English)
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T Freilinger
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M Bohe
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B Wegener
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B Müller-Myhsok
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M Dichgans
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H Knoblauch
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14 February 2008
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28
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4
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403-407
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