A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators-Reference-Cited by-同舟云学术

A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators

Published:2018-12-17 Issue: Volume: Page:
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Shin Dong Hoon¹,Jung Jinsei²,Koh Young Ik¹,Rim John Hoon¹,Lee Joon Suk¹,Choi Hye Ji²,Joo Sun Young¹,Yu Seyoung¹,Cha Do Hyeon³,Lee Seung Yeon³,Lee Ji Hyun⁴,Lee Min Goo¹^ORCID,Choi Jae Young²,Gee Heon Yung¹^ORCID

Affiliation:

1. Department of PharmacologyBrain Korea 21 PLUS Project for Medical SciencesYonsei University College of Medicine Seoul 03722 Korea

2. Department of OtorhinolaryngologyBrain Korea 21 PLUS Project for Medical SciencesYonsei University College of Medicine Seoul 03722 Korea

3. Yonsei University College of Medicine Seoul 03722 Korea

4. Department of DermatologySeoul St. Mary's HospitalCollege of MedicineThe Catholic University of Korea Seoul 03722 Korea

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.23698

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