Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia. (2010)

First Author: Vermeer S

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2010.10.015

PubMed Identifier: 21092923

Publication URI: http://europepmc.org/abstract/MED/21092923

Type: Journal Article/Review

Volume: 87

Parent Publication: American journal of human genetics

Issue: 6

ISSN: 0002-9297