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Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss.
Kalay, E; Karaguzel, A; Caylan, R; Heister, A; Cremers, F P M; Cremers, C W R J; Brunner, H G; de Brouwer, A P M; Kremer, H.
Affiliation
  • Kalay E; Department of Human Genetics, Radboud University, Nijmegen Medical Centre, Nijmegen, The Netherlands. E.Kalay@antrg.umcn.nl
Hum Mutat ; 26(6): 591, 2005 Dec.
Article in En | MEDLINE | ID: mdl-16287143
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Collection: 01-internacional Database: MEDLINE Main subject: Frameshift Mutation / Mutation, Missense / Hearing Loss / Membrane Proteins Type of study: Prognostic_studies Limits: Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2005 Document type: Article Affiliation country: Países Bajos Country of publication: Estados Unidos
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Frameshift Mutation / Mutation, Missense / Hearing Loss / Membrane Proteins Type of study: Prognostic_studies Limits: Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2005 Document type: Article Affiliation country: Países Bajos Country of publication: Estados Unidos