1. A novel familial mutation in the PCSK1 gene that alters the oxyanion hole residue of proprotein convertase 1/3 and impairs its enzymatic activity.

Author:

Library: Center and Library of Islamic Studies in European Languages (Qom)

2. Applications of Next-Generation DNA Sequencing to the Identification of Rare Variants in Congenital Disorders of the Intestine and Brain

Author:

Library: Center and Library of Islamic Studies in European Languages (Qom)