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

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Identification of three novel polymorphisms in the MJD1 gen and study of their frequency in the Portuguese population
Segregation distortion of wild-type alleles at the Machado-Joseph disease locus : a study in normal families from the Azores islands (Portugal)
Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine
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
The CAG repeat at the Huntington disease gene in the Portuguese population : insights into its dynamics and to the origin of the mutation
A novel H101Q mutation causes PKCγ loss in spinocerebellar ataxia type 14

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