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Origin of the SCA7 gene mutation in South Africa: implications for molecular diagnostics

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Published in:	Clinical genetics 2006-11, Vol.70 (5), p.415-417
Main Authors:	Greenberg, J, Solomon, GAE, Vorster, AA, Heckmann, J, Bryer, A
Format:	Article
Language:	English
Subjects:	African Continental Ancestry Group - genetics Alleles Ataxin-7 Case-Control Studies Female Founder Effect Gene Frequency Haplotypes Humans Linkage Disequilibrium Male Microsatellite Repeats Mutation Nerve Tissue Proteins - genetics Pedigree Polymorphism, Single Nucleotide South Africa Spinocerebellar Ataxias - diagnosis Spinocerebellar Ataxias - genetics
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creator	Greenberg, J Solomon, GAE Vorster, AA Heckmann, J Bryer, A
description
doi_str_mv	10.1111/j.1399-0004.2006.00680.x
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subjects	African Continental Ancestry Group - genetics Alleles Ataxin-7 Case-Control Studies Female Founder Effect Gene Frequency Haplotypes Humans Linkage Disequilibrium Male Microsatellite Repeats Mutation Nerve Tissue Proteins - genetics Pedigree Polymorphism, Single Nucleotide South Africa Spinocerebellar Ataxias - diagnosis Spinocerebellar Ataxias - genetics
title	Origin of the SCA7 gene mutation in South Africa: implications for molecular diagnostics
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