LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss

出版年份 2018 全文链接

标题

作者

关键词

Deafness, Homozygosity mapping, Exome sequencing, LHFPL5

出版物

Volume -, Issue -, Pages -

出版商

Elsevier BV

发表日期

2018-11-23

DOI

10.1016/j.ejmg.2018.11.026

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