MYO1F as a candidate gene for nonsyndromic deafness, DFNB15

Archives of Otolaryngology - Head and Neck Surgery

Volumn 127, Issue 8, 2001, Pages 921-925

  Chen, Achih H ^a   Stephan, Dietrich A ^b   Hasson, Tama ^c   Fukushima, Kunihiro ^d   Nelissen, Christiana M ^a   Chen, Arthur F ^a   Jun, Andrew I ^a   Ramesh, Arabandi ^e   Van Camp, Guy ^f   Smith, Richard J H ^a  

^a UNIVERSITY OF IOWA   (United States)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^c YALE UNIVERSITY   (United States)

^d OKAYAMA UNIVERSITY MEDICAL SCHOOL   (Japan)

^e UNIVERSITY OF MADRAS   (India)

^f UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 19P; CHROMOSOME 3Q; CHROMOSOME MAP; COCHLEA; DNA SEQUENCE; EXON; GENE EXPRESSION; GENE LOCUS; GENE MAPPING; HEARING IMPAIRMENT; HUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; POLYMERASE CHAIN REACTION; SEGREGATION ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0034893621     PISSN: 08864470     EISSN: None     Source Type: Journal    
DOI: 10.1001/archotol.127.8.921     Document Type: Article

References (22)

1. Linkage analysis in man
2. New gene for autosomal recessive nonsyndromic hearing loss maps to either chromosome 3q or 19p
3. Cloning of the genes encoding two murine and human cochlear unconventional type I myosins
4. Mapping of unconventional myosins in mouse and humans
5. Unconventional myosins
6. A type VIIA myosin encoded by the mouse deafness gene shaker-1
7. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells
8. Defective myosin VIIA gene responsible for Usher syndrome type 1B
9. Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene
10. Unconventional myosins
11. Unconventional myosins in inner-ear sensory epithelia
12. Mutations in the myosin VIIA gene cause nonsyndromic deafness
13. The autosomal recessive isolated deafness, DFNB2, and Usher 1B syndrome are allelic defects of the myosin-VIIA gene
14. A gene for a dominant form of nonsyndromic deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene
15. Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene
16. Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3
17. Organization of the human genome