GJB2 mutations in Turkish patients with ARNSHL: Prevalence and two novel mutations

Hearing Research

Volumn 203, Issue 1-2, 2005, Pages 88-93

  Kalay, Ersan ^a,b   Caylan, Refik ^b   Kremer, Hannie ^a   De Brouwer, Arjan P M ^a   Karaguzel, Ahmet ^b  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b KARADENIZ TECHNICAL UNIVERSITY   (Turkey)

Author keywords

35delG; Connexin 26; GJB2; GJB6; Hearing loss

Indexed keywords

CONNEXIN 26;

ALLELE; ARTICLE; AUTOSOMAL RECESSIVE NON SYNDROMIC HEARING LOSS; CHILD; DISEASE SEVERITY; GENE MUTATION; GENETIC DISORDER; GENETIC SCREENING; HEARING LOSS; HUMAN; INCIDENCE; MAJOR CLINICAL STUDY; NUCLEOTIDE SEQUENCE; PATIENT; PATIENT ABANDONMENT; POPULATION RESEARCH; PRIORITY JOURNAL; TURKEY (BIRD);

EID: 18044390304     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.heares.2004.11.022     Document Type: Article

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