about
Hereditary xanthinuria. Evidence for enhanced hypoxanthine salvage.Mechanism of excessive purine biosynthesis in hypoxanthine-guanine phosphoribosyltransferase deficiency.Developmental changes in purine phosphoribosyltransferases in human and rat tissues.Validation and steady-state analysis of a power-law model of purine metabolism in man.Lesch-Nyhan syndrome and its pathogenesis: purine concentrations in plasma and urine with metabolite profiles in CSF.
P2860
description
1968 nî lūn-bûn
@nan
1968 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1968 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1968年の論文
@ja
1968年論文
@yue
1968年論文
@zh-hant
1968年論文
@zh-hk
1968年論文
@zh-mo
1968年論文
@zh-tw
1968年论文
@wuu
name
Study of purine metabolism in a xanthinuric female.
@ast
Study of purine metabolism in a xanthinuric female.
@en
Study of purine metabolism in a xanthinuric female.
@nl
type
label
Study of purine metabolism in a xanthinuric female.
@ast
Study of purine metabolism in a xanthinuric female.
@en
Study of purine metabolism in a xanthinuric female.
@nl
prefLabel
Study of purine metabolism in a xanthinuric female.
@ast
Study of purine metabolism in a xanthinuric female.
@en
Study of purine metabolism in a xanthinuric female.
@nl
P2093
P2860
P356
P1476
Study of purine metabolism in a xanthinuric female.
@en
P2093
P2860
P304
P356
10.1172/JCI105824
P407
P577
1968-06-01T00:00:00Z