Dentatorubral-pallidoluysian atrophy in three generations, with clinical courses from nearly asymptomatic elderly to severe juvenile, in an Australian family of Macedonian descent-Reference-Cited by-同舟云学术

Dentatorubral-pallidoluysian atrophy in three generations, with clinical courses from nearly asymptomatic elderly to severe juvenile, in an Australian family of Macedonian descent

Published:2005 Issue:2 Volume:136A Page:201-204
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Vinton Anita,Fahey Michael C.,O'Brien Terence J.,Shaw Janet,Storey Elsdon,McKinlay Gardner R.J.,Mitchell Peter J.,Du Sart Desirée,King John O.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference22 articles.

1. Dentatorubral-pallidoluysian atrophy and Haw River syndrome

2. Molecular re-investigation of patients with Huntington's disease in Wessex reveals a family with dentatorubral and pallidoluysian atrophy

3. Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X

4. Genetic Analysis of a Dentatorubral-Pallidoluysian Atrophy Family: Relevance to Apparent Sporadic Cases.

5. Dentatorubral-pallidoluysian atrophy: Clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat

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