A new mutation in thePOU3F4gene in a japanese family with x-linked mixed deafness (DFN3)-Reference-Cited by-同舟云学术

A new mutation in thePOU3F4gene in a japanese family with x-linked mixed deafness (DFN3)

Published:1998-10 Issue:10 Volume:108 Page:1544-1547
ISSN:0023-852X
Container-title:The Laryngoscope
language:en
Short-container-title:Laryngoscope

Author:

Hagiwara Hideo,Tamagawa Yuya,Kitamura Ken,Kodera Kazuoki

Publisher

Wiley

Subject

Otorhinolaryngology

Reference13 articles.

1. Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4;de Kok;Science,1995

2. Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3;Bitner-Glindzicz;Hum Mol Genet,1995

3. Molecular analysis of the POU3F4 gene in patients with clinical and radiographic evidence of X-linked mixed deafness with perilymphatic gusher;Friedman;Ann Otol Rhinol Laryngol,1997

4. Computed tomographic diagnosis of X-linked congenital mixed deafness, fixation of the stapedial footplate, and perilymphatic gusher;Talbot;Am J Otol,1994

5. X-linked deafness, stapes gushers and a distinctive defect of the inner ear;Phelps;Neuroradiology,1991

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