KEGG   VARIANT: 36v1
Entry
36v1                      Variant                                  
Name
ACADSB deficiency
Gene
ACADSB  acyl-CoA dehydrogenase short/branched chain [KO:K09478]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 600301
Network
nt06024  Valine, leucine and isoleucine degradation
Disease
H00375  SBCAD deficiency
Reference
  Authors
Andresen BS, Christensen E, Corydon TJ, Bross P, Pilgaard B, Wanders RJ, Ruiter JP, Simonsen H, Winter V, Knudsen I, Schroeder LD, Gregersen N, Skovby F
  Title
Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism.
  Journal
Am J Hum Genet 67:1095-103 (2000)
DOI:10.1086/303105
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