Histopathologic features of the temporal bone in usher syndrome type I

Archives of Otolaryngology - Head and Neck Surgery

Volumn 126, Issue 8, 2000, Pages 1018-1023

  Wagenaar, Mariette ^a   Schuknecht, Harold ^b   Nadol Jr , Joseph ^b   Benraad Van Rens, Meeke ^c   Pieke Dahl, Sandra ^d   Kimberling, William ^d   Cremers, Cor ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

^c Institute for the Deaf and the Blind (Kalorama)   (Netherlands)

^d BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN;

ADULT; AGED; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; COCHLEAR NERVE; CORTI ORGAN; FEMALE; GENE MUTATION; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; MALE; PEDIGREE ANALYSIS; PERCEPTION DEAFNESS; TEMPORAL BONE; USHER SYNDROME;

EID: 0033840865     PISSN: 08864470     EISSN: None     Source Type: Journal    
DOI: 10.1001/archotol.126.8.1018     Document Type: Article

References (25)

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5. Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
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7. Localization of the Usher type I D gene (USH1D) to chromosome 10
8. A newly identiffed locus for Usher syndrome type I, USH1E, maps to chromosome 21q21
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24. Human myosin VIIA responsible for Usher 1B syndrome a predicted membrane associated motor protein expressed in developing sensory epithelia