A study of Huntington disease-like syndromes in black South African patients reveals a single SCA2 mutation and a unique distribution of normal alleles across five repeat loci-Reference-Cited by-同舟云学术

A study of Huntington disease-like syndromes in black South African patients reveals a single SCA2 mutation and a unique distribution of normal alleles across five repeat loci

Published:2018-07 Issue: Volume:390 Page:200-204
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Baine Fiona K.^ORCID,Peerbhai Nabeelah,Krause Amanda

Funder

National Health Laboratory Service Research Trust

South African Medical Research Council

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference40 articles.

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