Contribution of GJB2 mutations and Four common DFNB loci in autosomal recessive non-syndromic hearing impairment in Markazi and Qom provinces of Iran

Iranian Journal of Biotechnology

Volumn 7, Issue 2, 2009, Pages

  Sadeghi, Abdorrahim ^a,b,c   Sanati, Mohammad Hossein ^b   Alasti, Fatemeh ^b   Chaleshtori, Morteza Hashemzadeh ^d   Mahmoudian, Saeid ^e   Ataei, Mitra ^b  

^a TARBIAT MODARES UNIVERSITY   (Iran)

^b NATIONAL INSTITUTE OF GENETIC ENGINEERING AND BIOTECHNOLOGY   (Iran)

^c ARAK UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^d SHAHREKORD UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^e IRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

Autosomal recessive non syndromic hearing loss (ARNSHL); GJB2; Hearing impairment; Linkage analysis; Short Tandem Repeat (STR)

Indexed keywords

DNA;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; AUTOSOMAL RECESSIVE NONSYNDROMIC HEARING LOSS; CLINICAL ARTICLE; CONGENITAL DEAFNESS; FAMILY STUDY; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; HEARING IMPAIRMENT; HEARING LOSS; HUMAN; IRAN; MALE; NUCLEOTIDE SEQUENCE; PEDIGREE ANALYSIS; POLYMERASE CHAIN REACTION; SHORT TANDEM REPEAT;

EID: 69149102898     PISSN: 17283043     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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