Clinical presentation of DFNB12 and Usher syndrome type 1D.

Advances in oto-rhino-laryngology

Volumn 61, Issue , 2002, Pages 145-152

  Bork, Julie M ^a   Morell, Robert J ^a   Khan, Shaheen ^a   Riazuddin, Sheikh ^a   Wilcox, Edward R ^a   Friedman, Thomas B ^a   Griffith, Andrew J ^a  

^a NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CADHERIN; CDH23 PROTEIN, HUMAN;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; FEMALE; GENETIC LINKAGE; GENETICS; HUMAN; MALE; MIDDLE AGED; MISSENSE MUTATION; PERCEPTION DEAFNESS; PHENOTYPE; PRESCHOOL CHILD; RETINITIS PIGMENTOSA; SYNDROME; VESTIBULAR DISORDER;

ADOLESCENT; ADULT; AGED; CADHERINS; CHILD; CHILD, PRESCHOOL; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; LINKAGE (GENETICS); MALE; MIDDLE AGED; MUTATION, MISSENSE; PHENOTYPE; RETINITIS PIGMENTOSA; SYNDROME; VESTIBULAR DISEASES;

MLCS; MLOWN;

EID: 0036362711     PISSN: 00653071     EISSN: None     Source Type: Journal    
DOI: 10.1159/000066829     Document Type: Article

References (0)