Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts
GCNT2基因位点缺失导致常染色体隐性遗传性先天性白内障
期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0167562
Irum, Bushra; Khan, Shahid Y; Ali, Muhammad; Daud, Muhammad; Kabir, Firoz; Rauf, Bushra; Fatima, Fareeha; Iqbal, Hira; Khan, Arif O; Al Obaisi, Saif; Naeem, Muhammad Asif; Nasir, Idrees A; Khan, Shaheen N; Husnain, Tayyab; Riazuddin, Sheikh; Akram, Javed; Eghrari, Allen O; Riazuddin, S Amer