Identification of three novel mutations in human EYA1 protein associated with Branchio-Oto-Renal syndrome.

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Title:	Identification of three novel mutations in human EYA1 protein associated with Branchio-Oto-Renal syndrome.
Author(s):	Kumar, S.; Kimberling, W.J.; Weston, M.D.; Schaefer, B.G.; Berg, M.A.; Marres, H.A.M. ; Cremers, C.W.R.J.
Publication year:	1998
Source:	Human Mutation, vol. 11, (1998), pp. 443-449
ISSN:	1059-7794
DOI:	https://doi.org/10.1002/(SICI)1098-1004(1998)11:6<443::AID-HUMU4>3.3.CO;2-J
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/188786
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Subject:	Genetics of hearing Erfelijk gehoorverlies
Organization:	Otorhinolaryngology
Journal title:	Human Mutation
Volume:	vol. 11
Page start:	p. 443
Page end:	p. 449