Pitfalls in molecular diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia

por Kolahdouz, Mahsa, Mohammadi, Zahra, Kolahdouz, Parisa, Tajamolian, Masoud, Khanahmad, Hossein
Publicado 2015

A Rare Missense Mutation and a Polymorphism with High Frequency in LDLR Gene among Iranian Patients with Familial Hypercholesterolemia

por Tajamolian, Masoud, Kolahdouz, Parisa, Nikpour, Parvaneh, Forouzannia, Seyed Khalil, Sheikhha, Mohammad Hasan, Yazd, Ehsan Farashahi
Publicado 2018