Dihydropteridine reductase deficiency: The first Moroccan case report-Reference-Cited by-同舟云学术

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Dihydropteridine reductase deficiency: The first Moroccan case report

Published:2024-06 Issue:2 Volume:2 Page:100008
ISSN:2950-2217
Container-title:Brain and Development Case Reports
language:en
Short-container-title:Brain and Development Case Reports

Author:

Khabbache Kaoutar,Lamzouri Afaf,Imlahi Hanaa,Oulmaati Abdallah

Publisher

Elsevier BV

Reference15 articles.

1. Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies;Opladen;Orphanet J Rare Dis,2020

2. Dihydropteridine reductase deficiency in man: from biology to treatment;Ponzone;Med Res Rev.,2004

3. Insights into the expanding phenotypic spectrum of inherited disorders of biogenic amines;Kuseyri Hübschmann;Nat Commun,2021

4. Disorders of tetrahydrobiopterin metabolism and their treatment;Shintaku;Curr Drug Metab,2002

5. Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE);Romstad;Hum Genet,2000

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