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A case report of short-chain acyl-CoA dehydrogenase deficiency (SCADD)
BACKGROUND: Short-chain acyl-CoA dehydrogenase deficiency (SCADD) is a rare inherited mitochondrial fatty acid oxidation disorder associated with variations in the ACADS (Acyl-CoA dehydrogenase, C-2 to C-3 short chain) gene. SCADD has highly variable biochemical, genetic and clinical characteristics...
में बचाया:
| में प्रकाशित: | Biochem Med (Zagreb) |
|---|---|
| मुख्य लेखकों: | , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Croatian Society of Medical Biochemistry and Laboratory Medicine
2015
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4470102/ https://ncbi.nlm.nih.gov/pubmed/26110041 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11613/BM.2015.029 |
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