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Actin genes
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Functional analysis of cytoplasmic [gamma]-actin mutations causing non-syndromic, progressive autosomal dominant hearing loss
Korrapati, Soumya
Text (2009)
Part of
Electronic Theses & Dissertations
Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness]
Liang, Yong
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)
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