Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment (vol 65, pg 187, 2020)

被引：0
|
作者：
Liaqat, Khurram
Hussain, Shabir
Bilal, Muhammad
Nasir, Abdul
Acharya, Anushree
Ali, Raja Hussain
Nawaz, Shoaib
Umair, Muhammad
Schrauwen, Isabelle
Ahmad, Wasim
Leal, Suzanne M.
机构：
[1] Quaid-i-Azam University,Department of Biotechnology, Faculty of Biological Sciences
[2] Baylor College of Medicine,Center of Statistical Genetics, Department of Molecular and Human Genetics
[3] Quaid-i-Azam University,Department of Biochemistry, Faculty of Biological Sciences
[4] Ajou University,Department of Molecular Science and Technology
[5] Columbia University Medical Center,Center for Statistical Genetics, Gertrude H. Sergievsky Center, Taub Institute for Alzheimer’s Disease and the Aging Brain, Department of Neurology
[6] Boston Children’s Hospital,Division of Hematology/Oncology
[7] King Saud bin Abdulaziz University for Health Science,Medical Genomics Research Department, King Abdullah International Medical Research Center (KAIMRC)
[8] Ministry of National Guard-Health Affairs (MNGHA),undefined
来源：
JOURNAL OF HUMAN GENETICS | 2022年 / 67卷 / 03期
关键词：
D O I：
10.1038/s10038-021-00951-9
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：181 / 181
页数：1
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