Mammalian cochlear genes and hereditary deafness

Microbial and Comparative Genomics

Volumn 5, Issue 2, 2000, Pages 61-69

  Shastry, B S ^a  

^a OAKLAND UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; CLINICAL OBSERVATION; ENVIRONMENTAL FACTOR; GENE LOCUS; GENETIC DISORDER; HEARING IMPAIRMENT; HUMAN; MOUSE; MULTIFACTORIAL GENETIC DISORDER; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; SHORT SURVEY; TREATMENT OUTCOME;

ANIMALIA; MAMMALIA;

EID: 0033758176     PISSN: 10906592     EISSN: None     Source Type: Journal    
DOI: 10.1089/10906590050179747     Document Type: Short Survey

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3. Here come more genes
4. The mouse snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells
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34. The fundamental and medical impacts of recent progress in research on hereditary hearing loss
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47. Mutation in COL 11A2 gene cause nonsyndromic hearing loss (DFNA 13)
48. Unconventional myosins in cell movement, membrane traffic and signal transduction
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67. Mutations in the human alpha-tectorin gene cause autosomal dominant nonsyndromic hearing impairment
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69. The autosoreal recessive isolated deafness, DFNB2 and the Usher 1B Syndrome are allelic defects of the myosin VIIA gene
70. Human myosin VIIA responsible for the Usher 1B syndrome: A predicted membrane-associated motor protein expressed in developing sensory epithelia
71. Myosin 7A mutation screening in 189 Usher syndrome type I patients
72. A mutation in OTOF, encoding otoferlin,a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness