The First Reported Case of a Child with Two Different Rare Metabolic Disorders: Very Long-Chain Acyl-CoA Dehydrogenase Deficiency and Encephalomyopathic Mitochondrial DNA Depletion Syndrome 13

The First Reported Case of a Child with Two Different Rare Metabolic Disorders: Very Long-Chain Acyl-CoA Dehydrogenase Deficiency and Encephalomyopathic Mitochondrial DNA Depletion Syndrome 13

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Veröffentlicht in:Global medical genetics 2023, Vol.10 (4), p.278-281
Hauptverfasser: Alotaibi, Maha, Alqasmi, Amal, Albassam, Faisal, Alkahtani, Turki, Alqahtany, Muath, Alkhaldi, Mohammed
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container_title Global medical genetics
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creator Alotaibi, Maha
Alqasmi, Amal
Albassam, Faisal
Alkahtani, Turki
Alqahtany, Muath
Alkhaldi, Mohammed
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doi_str_mv 10.1055/s-0043-1775979
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title The First Reported Case of a Child with Two Different Rare Metabolic Disorders: Very Long-Chain Acyl-CoA Dehydrogenase Deficiency and Encephalomyopathic Mitochondrial DNA Depletion Syndrome 13
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