Identification of two pax3 mutations causing Waardenburg syndrome, one within the paired domain (M62V) and the other downstream of the homeodomain (Q282X).

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Title:	Identification of two pax3 mutations causing Waardenburg syndrome, one within the paired domain (M62V) and the other downstream of the homeodomain (Q282X).
Author(s):	Hol, F.A. ; Geurds, M.P.A.; Cremers, C.W.R.J. ; Hamel, B.C.J. ; Mariman, E.C.M.
Publication year:	1998
Source:	Human Mutation, vol. 1, (1998), pp. S145-S147
ISSN:	1059-7794
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/166810
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Subject:	Genetics of hearing Erfelijk gehoorverlies
Organization:	Human Genetics Otorhinolaryngology
Journal title:	Human Mutation
Volume:	vol. 1
Page start:	p. S145
Page end:	p. S147