Identification of a novel frameshift mutation in the DFNB31/WHRN gene in a Tunisian consanguineous family with hereditary non-syndromic recessive hearing loss.

Human mutation

Volumn 25, Issue 5, 2005, Pages 503-

  Tlili, Abdelaziz ^a   Charfedine, Ilhem ^a   Lahmar, Imed ^a   Benzina, Zaineb ^a   Mohamed, Ben Amor ^a   Weil, Dominique ^a   Idriss, Nabil ^a   Drira, Mohamed ^a   Masmoudi, Saber ^a   Ayadi, Hammadi ^a  

^a UNIVERSITY OF SFAX   (Tunisia)

Author keywords

[No Author keywords available]

Indexed keywords

DFNB31 PROTEIN, HUMAN; MEMBRANE PROTEIN;

ARTICLE; CONSANGUINITY; ETHNOLOGY; FEMALE; FRAMESHIFT MUTATION; GENETIC LINKAGE; GENETICS; HAPLOTYPE; HEARING LOSS; HUMAN; MALE; NUCLEOTIDE SEQUENCE; PEDIGREE; TUNISIA;

CONSANGUINITY; DNA MUTATIONAL ANALYSIS; FEMALE; FRAMESHIFT MUTATION; HAPLOTYPES; HEARING LOSS; HUMANS; LINKAGE (GENETICS); MALE; MEMBRANE PROTEINS; PEDIGREE; TUNISIA;

EID: 33144483509     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9333     Document Type: Article

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