A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations
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.
Published in European journal of pediatrics (01.06.2010)
Published in European journal of pediatrics (01.06.2010)
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