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Whole-exome sequencing identifies a novel missense variant within LOXHD1 causing rare hearing loss in a Chinese family

Abstract Background Deafness, autosomal recessive 77 (DFNB77) is a rare non-syndromic hearing loss (NSHL) worldwide, which is caused by deleterious variants within lipoxygenase homology domains 1 (LOXHD1). Here we identified that a novel missense variant of LOXHD1 was associated with NSHL in a Chine...

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Bibliographic Details
Main Authors:	Na Shen (Author), Ting Wang (Author), Delei Li (Author), Aiguo Liu (Author), Yanjun Lu (Author)
Format:	Book
Published:	BMC, 2019-02-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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