Title : Enzyme replacement prevents neonatal death, liver damage, and osteoporosis in murine homocystinuria.

Pub. Date : 2017 Dec

PMID : 28821635






2 Functional Relationships(s)
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1 Classical homocystinuria (HCU) is an inborn error of sulfur amino acid metabolism caused by deficient activity of cystathionine beta-synthase (CBS), resulting in an accumulation of homocysteine and a concomitant decrease of cystathionine and cysteine in blood and tissues. Cysteine cystathionine beta-synthase Mus musculus
2 Classical homocystinuria (HCU) is an inborn error of sulfur amino acid metabolism caused by deficient activity of cystathionine beta-synthase (CBS), resulting in an accumulation of homocysteine and a concomitant decrease of cystathionine and cysteine in blood and tissues. Cysteine cystathionine beta-synthase Mus musculus