Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10

OBJECTIVE: to map a mouse deafness gene, identify the underlying mutation and develop a mouse model for human deafness. METHODS: genetic linkage cross and genome scan were used to map a novel mutation named hypoplasia of the membranous labyrinth (hml), which causes hearing loss in mutant mice. RESUL...

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Main Authors: Zheng, Qing Yin, Harris, Belinda S, Ward-Bailey, Patricia F, Yu, Heping, Bronson, Roderick T, Davisson, Muriel T, Johnson, Kenneth R
Format: Artigo
Sprog:Inglês
Udgivet: 2004
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3004367/
https://ncbi.nlm.nih.gov/pubmed/21179397
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