Journal Article

A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

Inga Ebermann; Hendrik P. N. Scholl; Peter Charbel Issa; Elvir Becirovic; Jürgen Lamprecht; Bernhard Jurklies; José M. Millán; Elena Aller; Diana Mitter; Hanno Bolz

Human Genetics · Vol. 121, Issue 2 · pp. 203-211 · 2007

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Abstract

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Bibliographic Information

Journal	Human Genetics
Publisher	Springer
Publication Date	2007-03-12
Publication Year	2007
Volume	121
Issue	2
Pages	203-211
Document Type	Journal Article
Print ISSN	0340-6717
eISSN	1432-1203
DOI	10.1007/s00439-006-0304-0

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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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