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Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.
Bork, J M; Peters, L M; Riazuddin, S; Bernstein, S L; Ahmed, Z M; Ness, S L; Polomeno, R; Ramesh, A; Schloss, M; Srisailpathy, C R; Wayne, S; Bellman, S; Desmukh, D; Ahmed, Z; Khan, S N; Kaloustian, V M; Li, X C; Lalwani, A; Riazuddin, S; Bitner-Glindzicz, M; Nance, W E; Liu, X Z; Wistow, G; Smith, R J; Griffith, A J; Wilcox, E R; Friedman, T B; Morell, R J.
Affiliation
  • Bork JM; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, MD 20850, USA.
Am J Hum Genet ; 68(1): 26-37, 2001 Jan.
Article in En | MEDLINE | ID: mdl-11090341
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cadherins / Retinitis Pigmentosa / Deafness / Alleles / Genes, Recessive / Hearing Loss, Sensorineural / Mutation Limits: Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 2001 Type: Article Affiliation country: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cadherins / Retinitis Pigmentosa / Deafness / Alleles / Genes, Recessive / Hearing Loss, Sensorineural / Mutation Limits: Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 2001 Type: Article Affiliation country: United States