Literature DB >> 16283888

GJB2 gene mutations in Slovak hearing-impaired patients of Caucasian origin: spectrum, frequencies and SNP analysis.

G Minarik, E Ferakova, A Ficek, H Polakova, L Kadasi.   

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Year:  2005        PMID： 16283888     DOI： 10.1111/j.1399-0004.2005.00529.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  4 in total

1.  Single nucleotide polymorphisms of the GJB2 and GJB6 genes are associated with autosomal recessive nonsyndromic hearing loss.

Authors:  Ana Paula Grillo; Flávia Marcorin de Oliveira; Gabriela Queila de Carvalho; Ruan Felipe Vieira Medrano; Sueli Matilde da Silva-Costa; Edi Lúcia Sartorato; Camila Andréa de Oliveira
Journal:  Biomed Res Int       Date:  2015-05-17       Impact factor: 3.411

2.  Genetic Aetiology of Nonsyndromic Hearing Loss in Moravia-Silesia.

Authors:  Pavlina Plevova; Petra Tvrda; Martina Paprskarova; Petra Turska; Barbara Kantorova; Eva Mrazkova; Jana Zapletalova
Journal:  Medicina (Kaunas)       Date:  2018-05-04       Impact factor: 2.430

3.  Assessment of Gap Junction Protein Beta-2 rs3751385 Gene Polymorphism in Psoriasis Vulgaris.

Authors:  Elli-Anna Stylianaki; Anthony Karpouzis; Gregory Tripsianis; Stavroula Veletza
Journal:  J Clin Med Res       Date:  2019-09-01

4.  GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran.

Authors:  Ehsan Abbaspour Rodbaneh; Mohammad Panahi; Bahareh Rahimi; Haleh Mokabber; Reza Farajollahi; Behzad Davarnia
Journal:  J Clin Lab Anal       Date:  2021-09-28       Impact factor: 2.352
  4 in total

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