A novel missense mutation in the HAX1 gene in severe congenital neutropenia patients (Kostmann disease).M Faiyaz-Ul-Haque,A Al-Jefri, H A Abalkhail,M Toulimat, M A Al-Muallimi,M S Pulicat,A Gaafar,A A Alaiya,F Al-Dayel,I Peltekova,S H E ZaidiCLINICAL GENETICS(2009)引用 4|浏览1暂无评分关键词missense mutationAI 理解论文溯源树样例生成溯源树,研究论文发展脉络Chat Paper正在生成论文摘要