Evidence of a Common Founder for SCA12 in the Indian Population-Reference-Cited by-同舟云学术

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Evidence of a Common Founder for SCA12 in the Indian Population

Published:2005-09 Issue:5 Volume:69 Page:528-534
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Ann Human Genet

Author:

Bahl S.,Virdi K.,Mittal U.,Sachdeva M. P.,Kalla A. K.,Holmes S. E.,O'Hearn E.,Margolis R. L.,Jain S.,Srivastava A. K.,Mukerji M.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference14 articles.

1. Ethnic India: A Genomic View, With Special Reference to Peopling and Structure

2. SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study of an Indian family

3. Why is SCA12 different from other SCAs?

4. Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12

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