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Abbreviation : GJB2
Long Form : gap junction beta-2 protein
No. Year Title Co-occurring Abbreviation
2020 Analysis of miRNA-mRNA interaction network reveals gap junction beta 2 as a potential candidate gene involved in psoriatic hearing loss pathogenesis. Cx26, PASI
2019 Case report: Novel GJB2 variant c.113T>C associated with autosomal recessive non-syndromic hearing loss (ARNSHL) in a Han family. ARNSHL
2018 Analysis of mutation spectrum of common deafness-causing genes in Hakka newborns in southern China by semiconductor sequencing. GJB3, NSHL
2018 Update of spectrum c.35delG and c.-23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss. HL
2015 Cordblood-Based High-Throughput Screening for Deafness Gene of 646 Newborns in Jinan Area of China. GJB3, SLC26A4, UNHS
2015 Residual Hearing in DFNB1 Deafness and Its Clinical Implication in a Korean Population. ---