Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a German family with FHM1, cerebellar atrophy and mental retardation

Freilinger, Tobias; Bohe, M.; Wegener, Bernhard; Dichgans, Martin; Knoblauch, Hans

doi:10.1055/s-2007-987788

Akt Neurol

2007

DOI: 10.1055/s-2007-987788

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Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a German family with FHM1, cerebellar atrophy and mental retardation

Tobias Freilinger¹,

M. Bohe²,

Bernhard Wegener³

et al.

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Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a German family with FHM1, cerebellar atrophy and mental retardation

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