Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
2 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Genetic evaluation of hyperphenylalaninemia patients with tetrahydrobiopterin deficiency in Iranian population: Identification of four novel disease-causing variants.
Mol Genet Genomic Med. 2022 Dec;10(12):e2081. doi: 10.1002/mgg3.2081. Epub 2022 Nov 16.
Mol Genet Genomic Med. 2022.
PMID: 36382472
Free PMC article.
A Comprehensive Study of Disease-Causing Variants in PAH, QDPR, PTS, and PCD Genes in Iranian Patients with Hyperphenylalaninemia: A Systematic Review.
Ghanei M, Sadat Fatemi SH, Hamzehlouei T.
Ghanei M, et al. Among authors: sadat fatemi sh.
Hum Hered. 2023;88(1):8-17. doi: 10.1159/000529037. Epub 2023 Jan 16.
Hum Hered. 2023.
PMID: 36646061
Free PMC article.
Item in Clipboard
Cite
Cite