Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3-Reference-Cited by-同舟云学术

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

Published:1995 Issue:8 Volume:4 Page:1467-1469
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Bitner-Glindzicz Maria,Turnpenny Peter,Höglund Pia,Kääriäinen Helena,Sankila Eeva-Marja,van der Maarel Sylvere M.,de Kok Yvette J.M.,Ropers Hans-Hilger,Cremers Frans P.M.,Pembrey Marcus,Malcolm Susan

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/4/8/1467/2093889/4-8-1467.pdf

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