Deafness genes in families with non-syndromic hearing loss in Shandong, China: a genetic study

Hearing loss is the most frequent sensory disorder, affecting 1 in 500 newborns. More than 90 genes are associated with non-syndromic hearing loss. In this study we aimed to investigate the genetic etiology of families with non-syndromic hearing loss in Shandong, China.

Gespeichert in:
Autor*in:

Bai, Xiaohui [verfasserIn]

Xu, Lei

Zhang, Fengguo

Xiao, Yun

Li, Jianfeng

Wang, Haibo

Format:

E-Artikel

Sprache:

Englisch

Erschienen:

2016

Übergeordnetes Werk:

Enthalten in: Effects of shape functions on flexural–torsional buckling of fixed circular arches - Dou, Chao ELSEVIER, 2013, London [u.a.]

Übergeordnetes Werk:

volume:388 ; year:2016 ; pages:80

Links:

Volltext

DOI / URN:

10.1016/S0140-6736(16)32007-4

Katalog-ID:

ELV019047134

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