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Two new mutations, ESPN c.2257T>C and ESRRB c.10583 C>A, ca..:
Jihen Chouchen
;
Abdelaziz Tlili
http://www.hamdanjournal.org/article.asp?issn=2227-2437;year=2020;volume=13;issue=2;spage=115;epage=119;aulast=Chouchen. , 2020
Link:
https://doi.org/10.4103/HMJ.HMJ_92_19
RT Journal T1 <Title>Two new mutations, ESPN c.2257T>C and ESRRB c.10583 C>A, cause hearing loss in UAE families</Title> UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:68c8077e1be441a2bd6952859d30916d&Exemplar=1&LAN=DE A1 Jihen Chouchen A1 Abdelaziz Tlili PB Wolters Kluwer Medknow Publications YR 2020 K1 clinical exome sequencing K1 espn and esrrb genes K1 missense variant K1 splice-site dna variation K1 non-syndromic hearing loss K1 whole-exome sequencing K1 Medicine K1 R JF http://www.hamdanjournal.org/article.asp?issn=2227-2437;year=2020;volume=13;issue=2;spage=115;epage=119;aulast=Chouchen LK http://dx.doi.org/https://doi.org/10.4103/HMJ.HMJ_92_19 DO https://doi.org/10.4103/HMJ.HMJ_92_19 SF ELIB - SuUB Bremen
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