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Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes.
Schultz, Julie M; Bhatti, Rashid; Madeo, Anne C; Turriff, Amy; Muskett, Julie A; Zalewski, Christopher K; King, Kelly A; Ahmed, Zubair M; Riazuddin, Saima; Ahmad, Nazir; Hussain, Zawar; Qasim, Muhammad; Kahn, Shaheen N; Meltzer, Meira R; Liu, Xue Z; Munisamy, Murali; Ghosh, Manju; Rehm, Heidi L; Tsilou, Ekaterini T; Griffith, Andrew J; Zein, Wadih M; Brewer, Carmen C; Riazuddin, Sheikh; Friedman, Thomas B.
Affiliation
  • Schultz JM; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, MD 20850, USA.
J Med Genet ; 48(11): 767-75, 2011 Nov.
Article in En | MEDLINE | ID: mdl-21940737
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retina / Cadherins / Retinitis Pigmentosa / Vestibule, Labyrinth / Usher Syndromes / Hearing Loss, Sensorineural / Mutation Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Female / Humans / Male Country/Region as subject: America do norte Language: En Journal: J Med Genet Year: 2011 Type: Article Affiliation country: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retina / Cadherins / Retinitis Pigmentosa / Vestibule, Labyrinth / Usher Syndromes / Hearing Loss, Sensorineural / Mutation Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Female / Humans / Male Country/Region as subject: America do norte Language: En Journal: J Med Genet Year: 2011 Type: Article Affiliation country: United States