更正：GCNT2基因座缺失导致常染色体隐性先天性白内障。
Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.
作者信息
Irum Bushra, Khan Shahid Y, Ali Muhammad, Daud Muhammad, Kabir Firoz, Rauf Bushra, Fatima Fareeha, Iqbal Hira, Khan Arif O, Obaisi Saif Al, Naeem Muhammad Asif, Nasir Idrees A, Khan Shaheen N, Husnain Tayyab, Riazuddin Sheikh, Akram Javed, Eghrari Allen O, Riazuddin S Amer
出版信息
PLoS One. 2017 Mar 9;12(3):e0173719. doi: 10.1371/journal.pone.0173719. eCollection 2017.
Abstract
[This corrects the article DOI: 10.1371/journal.pone.0167562.].
摘要
[本文更正了文章的数字对象标识符：10.1371/journal.pone.0167562。]
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本文引用的文献
1
Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.GCNT2基因座的缺失导致常染色体隐性先天性白内障。
PLoS One. 2016 Dec 9;11(12):e0167562. doi: 10.1371/journal.pone.0167562. eCollection 2016.
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