High frequency of GJB2 gene mutations in Polish patients with prelingual nonsyndromic deafness.

scientific article published in January 2001

High frequency of GJB2 gene mutations in Polish patients with prelingual nonsyndromic deafness. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1089/109065701753145637
P698PubMed publication ID11551103

P50authorJerzy BalQ66901299
P2093author name stringE Obersztyn
W Wiszniewski
E Nowakowska-Szyrwinska
L Sobieszczanska-Radoszewska
P433issue2
P921main subjectdeafnessQ12133
P304page(s)147-148
P577publication date2001-01-01
P1433published inGenetic Testing and Molecular BiomarkersQ15753742
P1476titleHigh frequency of GJB2 gene mutations in Polish patients with prelingual nonsyndromic deafness
P478volume5

Reverse relations

cites work (P2860)
Q50353341A TMC1 (transmembrane channel-like 1) mutation (p.S320R) in a Polish family with hearing impairment.
Q79243195DNA sequence analysis of GJB2, encoding connexin 26: observations from a population of hearing impaired cases and variable carrier rates, complex genotypes, and ethnic stratification of alleles among controls
Q40105775Differentiation of organotypic epidermis in the presence of skin disease-linked dominant-negative Cx26 mutants and knockdown Cx26.
Q28217345GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review
Q38125413GJB2-associated hearing loss: systematic review of worldwide prevalence, genotype, and auditory phenotype
Q50357155Prevalence of DFNB1 mutations among cochlear implant users in Slovakia and its clinical implications.
Q45786541Prevalence of GJB2 mutations in the Silk Road region of China and a report of three novel variants
Q30898157Statistical study of 35delG mutation of GJB2 gene: a meta-analysis of carrier frequency
Q35929073The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population.

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