Project title
以次世代定序技術探研SLC26A4基因突變之致病機制並研發新治療策略
Internal ID
MOST103-2314-B002-171-MY3
Principal Investigator
Start Date
August 1, 2014
End Date
July 31, 2015
Organizations
Partner Organizations
Project Web Site
Exploring the Pathogenetic Mechanisms of SLC26A4 Mutations with Next Generation Sequencing and Developing Novel Therapeutic Strategies
Keywords
遺傳性聽損
SLC26A4基因
Pendrin
基因置換鼠
次世代定序
hereditary hearing impairment
SLC26A4
Pendred syndrome
next generation sequencing