PTEN gene mutations in patients with macrocephaly and classic autism: A systematic review

por Zahedi Abghari, Fateme, Moradi, Yousef, Akouchekian, Mansoureh
Publicado 2019

Characterization of Niemann-Pick diseases genes mutation spectrum in Iran and identification of a novel mutation in SMPD1 gene

por Zahedi Abghari, Fateme, Bayat, Fatemeh, Razipour, Masoumeh, Karimipoor, Morteza, Taghavi-Basmenj, Maryam, Zeinali, Sirous, Davoudi-Dehaghani, Elham
Publicado 2019