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Apparent homozygosity for a novel splicing variant in EPS8 causes congenital profound hearing loss |
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Titel: |
Apparent homozygosity for a novel splicing variant in EPS8 causes congenital profound hearing loss |
Auteur: |
Yu, Sha Chen, Wen-xia Zhang, Yun-Fei Ni, Yihua Lu, Ping Wang, Bin Wang, Yan Wu, Bingbing Ni, Qi Wang, Huijun Xu, Zheng-min |
Verschenen in: |
European journal of medical genetics |
Paginering: |
Jaargang 64 () nr. 12 pagina's p. |
Jaar: |
2021 |
Inhoud: |
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Uitgever: |
Elsevier Masson SAS |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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