Seyedeh Helia Sadat Fatemi
Overview
Explore the profile of Seyedeh Helia Sadat Fatemi including associated specialties, affiliations and a list of published articles.
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2
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1
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Recent Articles
1.
Ghanei M, Sadat Fatemi S, Hamzehlouei T
Hum Hered
. 2023 Jan;
88(1):8-17.
PMID: 36646061
Background: Hyperphenylalaninemia (HPA) is an autosomal recessive disorder that results from a deficiency in the phenylalanine hydroxylase enzyme (PAH) or from a flaw in the genes that are responsible for...
2.
Sadat Fatemi S, Eshraghi P, Ghanei M, Hamzehloei T
Mol Genet Genomic Med
. 2022 Nov;
10(12):e2081.
PMID: 36382472
Background: Hyperphenylalaninemia (HPA) is the most common inborn error of amino acid metabolism worldwide. At least 2% of HPA cases are caused by a deficiency in tetrahydrobiopterin (BH4) metabolism. Genes...