about
Type 1 hereditary tyrosinemia. Evidence for molecular heterogeneity and identification of a causal mutation in a French Canadian patientDifferent molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I)Liver tumors in children with metabolic disordersOral loading of homogentisic acid in controls and in obligate heterozygotes for hereditary tyrosinemia type IRegionalization in hereditary IgA nephropathy.Neonatal hypertyrosinemia and evidence for deficiency of ascorbic acid in Arctic and subarctic peoplesHepatorenal tyrosinemia.Hereditary tyrosinemia type I: strong association with haplotype 6 in French Canadians permits simple carrier detection and prenatal diagnosis.
P2860
Q24564762-15C946BA-A841-4B62-98F6-2DE7BA4F64E4Q24676845-8F53B7C3-5759-46E2-9520-5EB04BDE5064Q26770292-41B023E3-910B-4B83-9C04-3D91E82DFAF6Q28335698-19D9CF21-6440-41D1-B552-0471664E79DEQ35199135-0321AB2B-BE2A-4EFA-9BFB-F1852F17F4A8Q35959478-90491C90-623B-4DC6-AF6E-0649B7DA3913Q38017842-A453A68E-0A7F-408C-91DA-692F6F540A89Q42557586-AA08658E-1DE6-4D9A-8B4D-8F65017A15AA
P2860
description
1969 nî lūn-bûn
@nan
1969 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1969 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1969年の論文
@ja
1969年論文
@yue
1969年論文
@zh-hant
1969年論文
@zh-hk
1969年論文
@zh-mo
1969年論文
@zh-tw
1969年论文
@wuu
name
Hereditary tyrosinemia in a French Canadian isolate
@ast
Hereditary tyrosinemia in a French Canadian isolate
@en
type
label
Hereditary tyrosinemia in a French Canadian isolate
@ast
Hereditary tyrosinemia in a French Canadian isolate
@en
prefLabel
Hereditary tyrosinemia in a French Canadian isolate
@ast
Hereditary tyrosinemia in a French Canadian isolate
@en
P2860
P1476
Hereditary tyrosinemia in a French Canadian isolate
@en
P2093
P2860
P407
P577
1969-01-01T00:00:00Z