Journal Article

A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss

Claire J. Sineni; Muzeyyen Yildirim-Baylan; Shengru Guo; Vladimir Camarena; Gaofeng Wang; Suna Tokgoz-Yilmaz; Duygu Duman; Guney Bademci; Mustafa Tekin

Human Genetics · Vol. 138, Issue 10 · pp. 1071-1075 · 2019

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Bibliographic Information

Journal	Human Genetics
Publisher	Springer
Publication Date	2019-10-01
Publication Year	2019
Volume	138
Issue	10
Pages	1071-1075
Document Type	Journal Article
Print ISSN	0340-6717
eISSN	1432-1203
DOI	10.1007/s00439-019-02037-1

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NARA Access Coverage	1964-01-01~Current
Journal Homepage	https://www.springer.com/journal/439
Publisher Page	Open Publisher Page

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