Your browser doesn't support javascript.
loading
A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family.
Bai, Haihua; Yang, Xukui; Wu, Huiguang; Chen, Yujie; Liu, Yangjian; Wu, Qizhu.
BMC Med Genet ; 15: 34, 2014 Mar 19.
Article in En | MEDLINE | ID: mdl-25008054
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Extracellular Matrix Proteins / Genes, Dominant / Hearing Loss / Mutation Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Country/Region as subject: Asia Language: En Journal: BMC Med Genet Journal subject: GENETICA MEDICA Year: 2014 Document type: Article Country of publication: Reino Unido
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Extracellular Matrix Proteins / Genes, Dominant / Hearing Loss / Mutation Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Country/Region as subject: Asia Language: En Journal: BMC Med Genet Journal subject: GENETICA MEDICA Year: 2014 Document type: Article Country of publication: Reino Unido