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Molecular cloning of an unconventional myosin MYO15 and the identification of mutations of MYO15 responsible for human nonsyndromic deafness DFNB3
Wang, Aihui
Text (1999)
Part of
Electronic Theses & Dissertations
Exploring molecular mechanisms of human genetic diseases--two examples : autosomal dominant hearing loss (DFNA20/26) and autosomal recessive lysosomal storage disease, beta-mannosidosis
Zhu, Mei
Text (2007)
Part of
Electronic Theses & Dissertations
Investigating DFNA20 mutations in {OCLCbr#DE}-actin : studies in yeast, cell culture, and mouse
Drummond, Meghan Chapman
Text (2010)
Part of
Electronic Theses & Dissertations
Hereditary deafness and mast cell tumors in dogs : sequence analysis of candidate genes from the melanocyte development pathway
Zemke, Daniel
Text (2003)
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Electronic Theses & Dissertations
Characterization of a DFNB1 deletion allele in a Michigan kindred of German descent
Wilch, Ellen Shields
Text (2010)
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Electronic Theses & Dissertations
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