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por Ghalavand, Mohammad Amin, Asghari, Alimohamad, Farhadi, Mohammad, Taghizadeh-Hesary, Farzad, Garshasbi, Masoud, Falah, Masoumeh
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Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12

por Daneshi, Ahmad, Garshasbi, Masoud, Farhadi, Mohammad, Falavarjani, Khalil Ghasemi, Vafaee-Shahi, Mohammad, Almadani, Navid, Zabihi, MohammadSina, Ghalavand, Mohammad Amin, Falah, Masoumeh
Publicado 2023