Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

American Journal of Human Genetics

Volumn 68, Issue 1, 2001, Pages 26-37

  Bork, Julie M ^a   Peters, Linda M ^a   Riazuddin, Saima ^a,b   Ahmed, Zubair M ^a,b   Li, X Cindy ^a   Griffith, Andrew J ^a   Wilcox, Edward R ^a   Friedman, Thomas B ^a   Morell, Robert J ^a   Ahmed, Zahoor ^b   Khan, Shaheen N ^b   Riazuddin, Sheikh ^b  

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

^b UNIVERSITY OF THE PUNJAB   (Pakistan)

Author keywords

[No Author keywords available]

Indexed keywords

CADHERIN; COMPLEMENTARY DNA;

ALLELE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 10Q; COCHLEA; CONSANGUINITY; CONTROLLED STUDY; FRAMESHIFT MUTATION; GENE AMPLIFICATION; GENE EXPRESSION; GENE LOCUS; GENE SEQUENCE; HEARING IMPAIRMENT; HUMAN; HUMAN CELL; MISSENSE MUTATION; NORTHERN BLOTTING; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; USHER SYNDROME; VESTIBULAR DISORDER;

EID: 0035168168     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/316954     Document Type: Article

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