A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations
Titel:
A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations
Auteur:
Faiyaz-Ul-Haque, Muhammad Al-Jefri, Abdullah Al-Dayel, Fouad Bhuiyan, Jalaluddin A. K. M. Abalkhail, Hala A. Al-Nounou, Randa Al-Abdullatif, Ahmed Pulicat, Monogaran S. Gaafar, Ameera Alaiya, Ayodele A. Peltekova, Iskra Zaidi, Syed H. E.