Items where Author is "Hashemi, Motahare Sadat"

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Alamatsaz, Marzieh and Jalalypour, Farzaneh and Hashemi, Motahare Sadat and Shafeghati, Yousef and Nasr-Esfahani, Mohammad Hossein and Ghaedi, Kamran (2021) Compound heterozygous p. Arg949Trp and p. Gly970Ala mutations deteriorated the function of PEX1p: a study on PEX1 in a patient with Zellweger syndrome. Journal of Cellular Biochemistry, 122 (9). pp. 1229-1238. ISSN 0730-2312 (Print) 1097-4644 (Online)

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