A novel H101Q mutation causes PKCγ loss in spinocerebellar ataxia type 14

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Identification of three novel polymorphisms in the MJD1 gen and study of their frequency in the Portuguese population
Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype
A novel H101Q mutation causes PKCγ loss in spinocerebellar ataxia type 14

スポンサーリンク