Characterization of the Human and Mouse Unconventional Myosin XV Genes Responsible for Hereditary Deafness DFNB3 and Shaker 2-Reference-Cited by-同舟云学术

Characterization of the Human and Mouse Unconventional Myosin XV Genes Responsible for Hereditary Deafness DFNB3 and Shaker 2

Published:1999-11 Issue:3 Volume:61 Page:243-258
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Liang Yong,Wang Aihui,Belyantseva Inna A.,Anderson David W.,Probst Frank J.,Barber Thomas D.,Miller Webb,Touchman Jeffrey W.,Jin Long,Sullivan Susan L.,Sellers James R.,Camper Sally A.,Lloyd Ricardo V.,Kachar Bechara,Friedman Thomas B.,Fridell Robert A.

Publisher

Elsevier BV

Subject

Genetics

Reference59 articles.

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3. Current Protocols in Molecular Biology;Ausubel,1991

4. Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice;Avraham;Hum. Mol. Genet.,1997

5. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells;Avraham;Nat. Genet.,1995

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