Journal Article

Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome

Nikki Liburd; Manju Ghosh; Saima Riazuddin; Sadaf Naz; Shaheen Khan; Zubair Ahmed; Sheikh Riazuddin; Yong Liang; Puthezhath Menon; Tenesha Smith; Ann Smith; Ken-Shiung Chen; James Lupski; Edward Wilcox; Lorraine Potocki; Thomas Friedman

Human Genetics · Vol. 109, Issue 5 · pp. 535-541 · 2001

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Abstract

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Bibliographic Information

Journal	Human Genetics
Publisher	Springer
Publication Date	2001-11-01
Publication Year	2001
Volume	109
Issue	5
Pages	535-541
Document Type	Journal Article
Print ISSN	0340-6717
eISSN	1432-1203
DOI	10.1007/s004390100604

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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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