Plasma cholesterol in adults with phenylketonuria
© 2015 Royal College of Pathologists of Australasia. Phenylketonuria (PKU) is an autosomal recessive disorder of phenylalanine (Phe) catabolism resulting from a deficiency of L-phenylalanine hydroxylase (PAH). An association between hyperphenylalaninaemia (HPA) and hypocholesterolaemia has been repo...
| Main Authors: | , , , , |
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| Format: | Journal Article |
| Published: |
Lippincott Williams and Wilkins
2015
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| Online Access: | http://hdl.handle.net/20.500.11937/39144 |