A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations von 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.

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One‐step synthesis of radioactive acyl‐CoA and acylcarnitines using rat liver mitochondrial outer membrane as enzyme source von Jalaluddin Bhuiyan, A. K. M., Pande, S. V.

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Carnitine palmitoyltransferase activities: effects of serum albumin, acyl-CoA binding protein and fatty acid binding protein von Bhuiyan, A K, Pande, S V

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