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1 Ergebnisse
1
Case Report: Novel Heterozygous DFNA5 Splicing Variant Resp..:
Xi Chen
;
Bao-Long Jia
;
Mei-Hui Li
..
https://www.frontiersin.org/article/10.3389/fgene.2020.569284/full. , 2020
Link:
https://doi.org/10.3389/fgene.2020.569284
RT Journal T1 <Title>Case Report: Novel Heterozygous DFNA5 Splicing Variant Responsible for Autosomal Dominant Non-syndromic Hearing Loss in a Chinese Family</Title> UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:d3affcfe2841463ebea22da4c9fdbe3d&Exemplar=1&LAN=DE A1 Xi Chen A1 Bao-Long Jia A1 Mei-Hui Li A1 Yuan Lyu A1 Cai-Xia Liu PB Frontiers Media S.A. YR 2020 K1 DFNA5 K1 hearing loss K1 mutation K1 exome sequencing K1 ADNSHL K1 Genetics K1 QH426-470 JF https://www.frontiersin.org/article/10.3389/fgene.2020.569284/full LK http://dx.doi.org/https://doi.org/10.3389/fgene.2020.569284 DO https://doi.org/10.3389/fgene.2020.569284 SF ELIB - SuUB Bremen
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