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Whole exome sequencing, in silico and functional studies co..:
Mona Mahfood
;
Jihen Chouchen
;
Walaa Kamal Eddine Ahmad Mohamed
...
http://www.sciencedirect.com/science/article/pii/S1319562X21002977. , 2021
Link:
https://doi.org/10.1016/j.sjbs.2021.04.036
RT Journal T1
Whole exome sequencing, in silico and functional studies confirm the association of the GJB2 mutation p.Cys169Tyr with deafness and suggest a role for the TMEM59 gene in the hearing process
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:2b1bab4f441b4b9fa8905ee2048a2741&Exemplar=1&LAN=DE A1 Mona Mahfood A1 Jihen Chouchen A1 Walaa Kamal Eddine Ahmad Mohamed A1 Abdullah Al Mutery A1 Rania Harati A1 Abdelaziz Tlili PB Elsevier YR 2021 K1 Whole exome sequencing K1 GJB2 gene K1 Missense mutation K1 Non-syndromic hearing loss K1 Biology (General) K1 QH301-705.5 JF http://www.sciencedirect.com/science/article/pii/S1319562X21002977 LK http://dx.doi.org/https://doi.org/10.1016/j.sjbs.2021.04.036 DO https://doi.org/10.1016/j.sjbs.2021.04.036 SF ELIB - SuUB Bremen
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