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Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment.
Gene ; 527(2): 537-40, 2013 Sep 25.
Article in En | MEDLINE | ID: mdl-23850727

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Membrane Glycoproteins / Codon, Nonsense / Alleles / Hearing Disorders Type of study: Prognostic_studies Limits: Child, preschool / Humans / Male Language: En Journal: Gene Year: 2013 Document type: Article Affiliation country: Francia Country of publication: Países Bajos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Membrane Glycoproteins / Codon, Nonsense / Alleles / Hearing Disorders Type of study: Prognostic_studies Limits: Child, preschool / Humans / Male Language: En Journal: Gene Year: 2013 Document type: Article Affiliation country: Francia Country of publication: Países Bajos