Literature DB >> 10868222

DFNA15.

K B Avraham1.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2000        PMID： 10868222     DOI： 10.1159/000059091

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


× No keyword cloud information.
  1 in total

1.  Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding.

Authors:  Rob W J Collin; Ramesh Chellappa; Robert-Jan Pauw; Gert Vriend; Jaap Oostrik; Wendy van Drunen; Patrick L Huygen; Ronald Admiraal; Lies H Hoefsloot; Frans P M Cremers; Mengqing Xiang; Cor W R J Cremers; Hannie Kremer
Journal:  Hum Mutat       Date:  2008-04       Impact factor: 4.878
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.