受强制性开放获取政策约束的文章 - Mohammad Hadi Imanieh了解详情
可在其他位置公开访问的文章：5 篇
Clinical and genetic spectrum of glycogen storage disease in Iranian population using targeted gene sequencing
Z Beyzaei, F Ezgu, B Geramizadeh, MH Imanieh, M Haghighat, ...
Scientific reports 11 (1), 7040, 2021
强制性开放获取政策： UK Medical Research Council
A new ATP7B gene mutation with severe condition in two unrelated Iranian families with Wilson disease
H Dastsooz, SM Dehghani, MH Imanieh, M Haghighat, M Moini, ...
Gene 514 (1), 48-53, 2013
强制性开放获取政策： US National Institutes of Health
A pathogenic variant of TULP3 causes renal and hepatic fibrocystic disease
H Jafari Khamirani, VR Palicharla, SA Dastgheib, M Dianatpour, ...
Frontiers in Genetics 13, 1021037, 2022
强制性开放获取政策： US National Institutes of Health
Identification of a novel mutation in the PHKA2 gene in a child with liver cirrhosis
Z Beyzaei, F Ezgu, MH Imanieh, B Geramizadeh
Journal of Pediatric Endocrinology and Metabolism 35 (3), 417-420, 2022
强制性开放获取政策： UK Medical Research Council
Mutation spectrum of Tyrosinemia type I in Iran, A retrospective cohort study
Z Beyzaei, Z Goudarzi, SM Dehghani, H Moravej, MH Imanieh, ...
European Journal of Medical Genetics 71, 104970, 2024
强制性开放获取政策： UK Medical Research Council
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