Pages that link to "Q68313011"
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The following pages link to The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the gene (Q68313011):
Displaying 13 items.
- Three RFLPs defining a haplotype associated with the common mutation in human medium-chain acyl-CoA dehydrogenase (MCAD) deficiency occur in Alu repeats. (Q35194683) (← links)
- Estimation of the incidence of a rare genetic disease through a two-tier mutation survey (Q35194753) (← links)
- A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD). (Q35195005) (← links)
- Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) gene (Q35279415) (← links)
- Disease-causing mutations in exon 11 of the medium-chain acyl-CoA dehydrogenase gene (Q35889170) (← links)
- Methods for the investigation of hypoglycaemia with particular reference to inherited disorders of mitochondrial beta-oxidation (Q40850490) (← links)
- Mammalian mitochondrial beta-oxidation (Q41280085) (← links)
- Molecular genetic characterization and urinary excretion pattern of metabolites in two families with MCAD deficiency due to compound heterozygosity with a 13 base pair insertion in one allele (Q42282561) (← links)
- Molecular basis of inherited medium-chain acyl-CoA dehydrogenase deficiency causing sudden child death (Q44609443) (← links)
- Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency due to heterozygosity for the common mutation and an allele resulting in low levels of MCAD mRNA (Q61763890) (← links)
- The A985G mutation in the medium-chain acyl-CoA dehydrogenase gene: high prevalence in the Swiss population resident in Geneva (Q70994525) (← links)
- Most cases of medium-chain acyl-CoA dehydrogenase deficiency escape detection in France (Q71482764) (← links)
- Scottish frequency of the common G985 mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene and the role of MCAD deficiency in sudden infant death syndrome (SIDS) (Q72290273) (← links)