Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3

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Title:	Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3
Author(s):	Bitner-Glindzicz, M.; Turnpenny, P.; Höglund, P.; Kääriäinen, H.; Sankila, E.M.; Maarel, S.M. van der; Kok, Y.J.M. de; Ropers, H.-H.; Cremers, F.P.M. ; Pembrey, M.; Malcolm, S.
Publication year:	1995
Source:	Human Molecular Genetics, vol. 4, iss. 8, (1995), pp. 1467-1469
ISSN:	0964-6906
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/22078
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Organization:	Human Genetics
Journal title:	Human Molecular Genetics
Volume:	vol. 4
Issue:	iss. 8
Page start:	p. 1467
Page end:	p. 1469
Languages used:	en

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