Journal Article

Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing loss

Kevin T. Booth; Amama Ghaffar; Muhammad Rashid; Luke T. Hovey; Mureed Hussain; Kathy Frees; Erika M. Renkes; Carla J. Nishimura; Mohsin Shahzad; Richard J. Smith; Zubair Ahmed; Hela Azaiez; Saima Riazuddin

Human Genetics · Vol. 139, Issue 12 · pp. 1565-1574 · 2020

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Abstract

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Bibliographic Information

Journal	Human Genetics
Publisher	Springer
Publication Date	2020-12-01
Publication Year	2020
Volume	139
Issue	12
Pages	1565-1574
Document Type	Journal Article
Print ISSN	0340-6717
eISSN	1432-1203
DOI	10.1007/s00439-020-02197-5

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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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