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Q38684866-29BB3D29-A5C3-4B99-B6B8-CF89EA24512D
Q38684866-29BB3D29-A5C3-4B99-B6B8-CF89EA24512D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38684866-29BB3D29-A5C3-4B99-B6B8-CF89EA24512D
Heterozygous carriers of succinyl-CoA:3-oxoacid CoA transferase deficiency can develop severe ketoacidosis.
P2860
Q38684866-29BB3D29-A5C3-4B99-B6B8-CF89EA24512D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38684866-29BB3D29-A5C3-4B99-B6B8-CF89EA24512D
rank
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type
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Statement
wasDerivedFrom
12cc5d8a1dd7cfe8015ac54757d616c92267a375
P2860
Patients homozygous for the T435N mutation of succinyl-CoA:3-ketoacid CoA Transferase (SCOT) do not show permanent ketosis.