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Find link is a tool written by Edward Betts .
searching for Very-long-chain acyl-CoA dehydrogenase 10 found (12 total)
alternate case: very-long-chain acyl-CoA dehydrogenase
Very long-chain acyl-coenzyme A dehydrogenase deficiency
(1,061 words)
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genetic mutations in DNA. A change of the gene that codes for very long -chain -acyl -CoA -dehydrogenase (VLCAD) results in a deficiency or malfunction of the produced
ACADVL
(986 words)
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HF (Nov 1995). "Molecular basis of human mitochondrial very -long -chain acyl -CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood"
ACADL
(1,610 words)
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activation, and hepatic insulin resistance. In animals with very long -chain acyl -CoA dehydrogenase deficiency, LCAD and MCAD work to compensate for the reduced
List of causes of hypoglycemia
(1,265 words)
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syndrome Tumors Tyrosinaemia type 1 Urea cycle disorder Uremia Very -long -chain acyl -CoA dehydrogenase deficiency Visceral leishmaniasis Wiedemann-Beckwith syndrome
Very long chain fatty acid
(445 words)
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web}}: CS1 maint: multiple names: authors list (link) "Very long -chain acyl -CoA dehydrogenase deficiency". Genetics Home Reference, National Institutes
List of disorders included in newborn screening programs
(716 words)
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acyl-CoA dehydrogenase deficiency (MCAD) > 1 in 25,000 Very -long -chain acyl -CoA dehydrogenase deficiency (VLCAD) > 1 in 75,000 Trifunctional protein deficiency
TECR
(454 words)
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activity, acting on the CH-CH group of donors protein binding very -long -chain -acyl -CoA dehydrogenase activity oxidoreductase activity very-long-chain enoyl-CoA
ACAD9
(1,710 words)
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medium-chain-acyl-CoA dehydrogenase activity fatty-acyl-CoA binding very -long -chain -acyl -CoA dehydrogenase activity Cellular component mitochondrial inner membrane
ETFA
(2,140 words)
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displays decreased thermal stability and is overrepresented in very -long -chain acyl -CoA dehydrogenase -deficient patients with mild childhood presentation". Molecular
ETFB
(2,257 words)
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displays decreased thermal stability and is overrepresented in very -long -chain acyl -CoA dehydrogenase -deficient patients with mild childhood presentation". Molecular