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1 Ergebnisse
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Apparent homozygosity for a novel splicing variant in EPS8 ..:
Yu, Sha
;
Chen, Wen-xia
;
Zhang, Yun-Fei
...
European Journal of Medical Genetics. 64 (2021) 12 - p. 104362 , 2021
Link:
https://doi.org/10.1016/j.ejmg.2021.104362
RT Journal T1 <Title>Apparent homozygosity for a novel splicing variant in EPS8 causes congenital profound hearing loss</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ejmg.2021.104362&Exemplar=1&LAN=DE A1 Yu, Sha A1 Chen, Wen-xia A1 Zhang, Yun-Fei A1 Ni, Yihua A1 Lu, Ping A1 Wang, Bin A1 Wang, Yan A1 Wu, Bingbing A1 Ni, Qi A1 Wang, Huijun A1 Xu, Zheng-min PB Elsevier BV YR 2021 SN 1769-7212 JF European Journal of Medical Genetics VO 64 IS 12 SP 104362 LK http://dx.doi.org/https://doi.org/10.1016/j.ejmg.2021.104362 DO https://doi.org/10.1016/j.ejmg.2021.104362 SF ELIB - SuUB Bremen
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