Associated Papers
Deciphering genes associated with diffuse large B-cell lymphoma with lymphomatous effusions: A mutational accumulation scoring approach.
Abdollahi S et al.
Biomarker Research, 2021
34635181 (PubMed )
Supplement: 40364_2021_330_MOESM2_ESM.xlsx › ___1
Whole genome mapping and identification of single nucleotide polymorphisms of four Bangladeshi individuals and their functional significance.
Khan S et al.
Bmc Research Notes, 2021
33743798 (PubMed )
Supplement: 13104_2021_5514_MOESM4_ESM.zip › Supplementary_File_1A-1.xlsx › Supplementary_File_1A-1.exonic_
Gjb3 Gene Mutations in Non-Syndromic Hearing Loss of Bloch, Kurd, and Turkmen Ethnicities in Iran.
Aliazami F et al.
Iranian Journal of Public Health, 2020
Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden.
Adadey SM et al.
Life (basel, Switzerland), 2020
Coincidence of mutations in different connexin genes in Hungarian patients.
Tóth T et al.
International Journal of Molecular Medicine, 2007
[Congenital hearing loss. Molecular genetic diagnosis of connexin genes and genetic counselling].
Kunstmann E et al.
Hno, 2005
GJB2 mutations in keratitis-ichthyosis-deafness syndrome including its fatal form.
Janecke AR et al.
American Journal of Medical Genetics. Part A, 2005
Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in Austria.
Frei K et al.
Hearing Research, 2004
Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment.
Mhatre AN et al.
Clinical Genetics, 2003
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