Spectrum of genetic variants associated with maple syrup urine disease in the Middle East, North Africa, and Türkiye (MENAT): a systematic review

<h3>Background</h3><p dir="ltr">Maple syrup urine disease (MSUD) is a hereditary metabolic disorder caused by a deficiency in the branched-chain α-keto acid dehydrogenase (BCKD) enzymatic complex. The Middle East and North Africa, and Türkiye (MENAT) region has witnessed...

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Main Author:	Salma Younes (6424865) (author)
Other Authors:	Razan Elkahlout (22392133) (author), Houda Kilani (18543973) (author), Sarah Okashah (18282262) (author), Hussain Al Sharshani (22457677) (author), Zoulikha Rezoug (6742660) (author), Hatem Zayed (835448) (author), Nader Al-Dewik (4166527) (author)
Published:	2025
Subjects:	Biological sciences Genetics Biomedical and clinical sciences Medical biochemistry and metabolomics Health sciences Public health Maple syrup urine disease (MSUD) Genetic variants Genotype-phenotype correlations MENA
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Spectrum of genetic variants associated with maple syrup urine disease in the Middle East, North Africa, and Türkiye (MENAT): a systematic review

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