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Biochemical Genetics|April 16, 2025
Identification of the Mutations Spectrum in the Fumarylacetoacetate Hydrolase Gene in Tyrosinemia Type 1 Patients in Northeastern IranAmir-Hossein Yazdani, Fatemeh Keyfi, Saman Nahid, et al.
Orphanet Journal of Rare Diseases|February 26, 2025
Epidemiology of inherited metabolic disorders in newborn screening: insights from three years of experience in Southern IranLeila Salarian, Homa Ilkhanipoor, Anis Amirhakimi, et al.
Indian Pediatrics|January 6, 2023
Inborn Errors of Metabolism Associated With Autism Among Children: A Multicenter Study from IranHossein Moravej, Soroor Inaloo, Saman Nahid, et al.
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