| Literature DB >> 20483489 |
Yu-Fen Guo1, Yan-Li Wang, Bai-Cheng Xu, Xiao-Wen Liu, Yi-Ming Zhu, Fei-Fan Zhao, Yu-Bin Ji, Ying Zhou, Jian-Qiang Li, Qian Li, Da-Yong Wang, Qiu-Ju Wang.
Abstract
It is known that enlarged vestibular aqueduct syndrome is closely related to the SLC26A4 mutation. Up to date, more than 200 of SLC26A4 mutations have been described, and novel mutations are being continually identified in different countries and ethnic groups. In this study, two novel variations were identified in a Chinese family associated with enlarged vestibular aqueduct. The two novel substitutions, c.232T>C and c.2006A>T, were detected in exon 3 and exon 17 of the pendrin encoding gene, respectively. The T/C transversion at 232 nucleotide caused p.Y78H mutation while the A/T transversion at 2006 nucleotide caused p.D669V mutation. Copyright 2010 Elsevier Ireland Ltd. All rights reserved.Entities:
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Year: 2010 PMID: 20483489 DOI: 10.1016/j.ijporl.2010.04.005
Source DB: PubMed Journal: Int J Pediatr Otorhinolaryngol ISSN: 0165-5876 Impact factor: 1.675