A deletion on Chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidate
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/content/pdf/10.1007/s003350010010.pdf
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
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2. A Mutation in Myo15 Leads to Usher-Like Symptoms in LEW/Ztm-ci2 Rats;PLoS ONE;2011-03-29
3. Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31;Nature Genetics;2003-06-29
4. Identification, characterization and expression analysis of a new fibrillar collagen gene, COL27A1;Matrix Biology;2003-03
5. New behavioral mutant rat exhibiting circling behavior (clx) controlled by a sex-linked recessive gene;Congenital Anomalies;2002-09
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