Screening of hereditary deafness gene in newborns and correlation between homozygous mutation of c.109G＞A (p.V37I) in JB2 gene and clinical phenotype of deafness

WU Zhao-xia; LIANG Li-sheng; YUAN Gui-long; QIN Gui-feng; MAO Zhong-ying; LV Li-yin; DAI Qi-qiang

doi:10.3969/j.issn.1005-4057.2020.06.009

Home>Articles>Screening of hereditary deafness gene in newborns and correlation between homozygous mutation of c.109G＞A (p.V37I) in JB2 gene and clinical phenotype of deafness

DOI: 10.3969/j.issn.1005-4057.2020.06.009

Screening of hereditary deafness gene in newborns and correlation between homozygous mutation of c.109G＞A (p.V37I) in JB2 gene and clinical phenotype of deafness

WU Zhao-xia

LIANG Li-sheng

YUAN Gui-long

QIN Gui-feng

MAO Zhong-ying

LV Li-yin

DAI Qi-qiang

Machine-generated Keywords：

Publication Date：2020-12-28

Online Publishing Date：2025-08-15(First online date of this platform, not the publication date of the document)

Pages：4( 680-683 )

Journal of Guangdong Medical College

ISSN：1005-4057

Year, Vol.(Issue)：2020,38(6)