Literature DB >> 10868234

The ins and outs of X-linked deafness type 3.

F P Cremers1, C W Cremers, H H Ropers.   

Abstract

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Year:  2000        PMID： 10868234     DOI： 10.1159/000059101

Source DB:  PubMed          Journal:  Adv Otorhinolaryngol        ISSN： 0065-3071


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  5 in total

1.  Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafness.

Authors:  Abram P Vore; Eugene H Chang; Jane E Hoppe; Merlin G Butler; Shawnia Forrester; Michael C Schneider; Luke L H Smith; Daniel W Burke; Colleen A Campbell; Richard J H Smith
Journal:  Arch Otolaryngol Head Neck Surg       Date:  2005-12

2.  Characterization of new otic enhancers of the pou3f4 gene reveal distinct signaling pathway regulation and spatio-temporal patterns.

Authors:  Àlex Robert-Moreno; Silvia Naranjo; Elisa de la Calle-Mustienes; José Luis Gómez-Skarmeta; Berta Alsina
Journal:  PLoS One       Date:  2010-12-31       Impact factor: 3.240

3.  A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family.

Authors:  Wan Du; Ming-Kun Han; Da-Yong Wang; Bing Han; Liang Zong; Lan Lan; Ju Yang; Qi Shen; Lin-Yi Xie; Lan Yu; Jing Guan; Qiu-Ju Wang
Journal:  Chin Med J (Engl)       Date:  2017-01-05       Impact factor: 2.628

4.  Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families.

Authors:  Yu Su; Xue Gao; Sha-Sha Huang; Jing-Ning Mao; Bang-Qing Huang; Jian-Dong Zhao; Dong-Yang Kang; Xin Zhang; Pu Dai
Journal:  BMC Med Genet       Date:  2018-09-04       Impact factor: 2.103

5.  A novel mutation in POU3F4 in a Chinese family with X-linked non-syndromic hearing loss.

Authors:  Bang-Qing Huang; Jia-Ling Zeng; Yong-Yi Yuan; Pu Dai
Journal:  J Otol       Date:  2015-09-30
  5 in total

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