A study of Iraqi patients with homocysteine remethylation disorders in a tertiary pediatric centre

Background: Hyperhomocysteinemia is a group of inherited homocysteine metabolism disorders characterised by elevated blood homocysteine levels (total homocysteine >15 μM). Homocystinuria is classified into two main homocysteine metabolism disorders. Classical Homocystinuria is caused by a deficie...

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Bibliographic Details
Main Authors: Mays R. Al-Tai, Adel A. Kareem, Nebal W. Saadi, Tawfig Ben Omran, Ban A. Abdul Majeed, Ibrahim F. Ibrahim, Lamia A. Alattar
Format: Article
Language:English
Published: Elsevier 2025-06-01
Series:Molecular Genetics and Metabolism Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2214426925000321
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