Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness.

scientific article published on 21 March 2007

Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.IJPORL.2007.02.007
P8608Fatcat IDrelease_geyhd26wjjaovlvsdrp3u5wf4a
P698PubMed publication ID17368814

P50authorMortaza BonyadiQ57054577
P2093author name stringMohsen Esmaeili
Mohammad Nejadkazem
P433issue6
P921main subjectdeafnessQ12133
hearing lossQ16035842
P304page(s)869-873
P577publication date2007-03-21
P1433published inInternational Journal of Pediatric OtorhinolaryngologyQ2602426
P1476titleCommon mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness
P478volume71

Reverse relations

cites work (P2860)
Q44001634A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients
Q89750482Analyses of del(GJB6-D13S1830) and del(GJB6-D13S1834) deletions in a large cohort with hearing loss: Caveats to interpretation of molecular test results in multiplex families
Q42759605Connexin 26 gene mutations in non-syndromic hearing loss among Kuwaiti patients
Q41608836Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran
Q41824758EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus
Q92514506Frequency of GJB2 mutations, GJB6-D13S1830 and GJB6-D13S1854 deletions among patients with non-syndromic hearing loss from the central region of Iran
Q44648339GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population
Q50354805GJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss
Q41683194GJB2 mutations in deaf population of Ilam (Western Iran): a different pattern of mutation distribution.
Q37782545Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations
Q90380905Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations
Q37973278Genetics of hearing loss: where are we standing now?
Q90116929Genetics of hereditary hearing loss in east Iran population: A systematic review of GJB2 mutations
Q50356398Identification of four novel connexin 26 mutations in non-syndromic deaf patients: genotype-phenotype analysis in moderate cases

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