Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy
Shaikh, Rehan S, Reuter, Peggy, Sisk, Robert A, Kausar, Tasleem, Shahzad, Mohsin, Maqsood, Muhammad I, Yousif, Ateeq, Ali, Muhammad, Riazuddin, Saima, Wissinger, Bernd, Ahmed, Zubair MVolume:
23
Language:
english
Journal:
European Journal of Human Genetics
DOI:
10.1038/ejhg.2014.136
Date:
April, 2015
File:
PDF, 1.92 MB
english, 2015