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ArticleAnnals of Indian Academy of Neurology

3-Hydroxyisobutyryl-CoA Hydrolase (HIBCH) Deficiency Cases Diagnosed by Only HIBCH Gene Analysis and Novel Pathogenic Mutation.

Nafiye Emel Çakar et al.PubMed ↗Full text ↗Publisher ↗

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4 papers cite it

2023
2024
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Full record →Abstract, authors, funding and every citing paper · PMID 34447000