A rare homozygous ALX4 mutation in a Bangladeshi girl with frontonasal dysplasia type-2 (FND2)
一名孟加拉国女孩患有2型额鼻发育不良(FND2),其ALX4基因存在罕见的纯合突变。
期刊:Heliyon
影响因子:3.6
doi:10.1016/j.heliyon.2024.e34929
Goswami, Barna; Rahman, Asifur; Jahan, Iffat; Akter, Shahina; Banu, Tanjina Akhtar; Osman, Eshrar; Uzzaman, Mohammad Samir; Habib, Ahashan; Alam, Md Shamsul; Mohammad Abu Obaida, Abu Saleh; Hasan Sarkar, Md Murshed; Khan, Salim