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Functional and structural impact of 10 ACADM missense mutations on human medium chain acyl-Coa dehydrogenase - ScienceDirect
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Genotypic differences of MCAD deficiency in the Asian population: Novel genotype and clinical symptoms preceding newborn screening notification | Genetics in Medicine
![A novel mutation of the ACADM gene (c.145C>G) associated with the common c.985A>G mutation on the other ACADM allele causes mild MCAD deficiency: a case report – topic of research paper in A novel mutation of the ACADM gene (c.145C>G) associated with the common c.985A>G mutation on the other ACADM allele causes mild MCAD deficiency: a case report – topic of research paper in](https://cyberleninka.org/viewer_images/1512052/f/1.png)
A novel mutation of the ACADM gene (c.145C>G) associated with the common c.985A>G mutation on the other ACADM allele causes mild MCAD deficiency: a case report – topic of research paper in
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SciELO - Brasil - The value of fasting in the diagnosis of medium-chain acyl-CoA dehydrogenase deficiency The value of fasting in the diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
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ACADM mutations detected by sequence analysis. Compound heterozygote... | Download Scientific Diagram
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Liver ABCA1 and ACADM protein amounts are increased in huCETP mice.... | Download Scientific Diagram
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Genes | Free Full-Text | ACADM Frameshift Variant in Cavalier King Charles Spaniels with Medium-Chain Acyl-CoA Dehydrogenase Deficiency
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