Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase gene.
about
Primary hyperoxaluria type 1: a cluster of new mutations in exon 7 of the AGXT gene.Functional synergism between the most common polymorphism in human alanine:glyoxylate aminotransferase and four of the most common disease-causing mutationsCorrection of an enzyme trafficking defect in hereditary kidney stone disease in vitro.
P2860
Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase gene.
description
1994 nî lūn-bûn
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1994年の論文
@ja
1994年学术文章
@wuu
1994年学术文章
@zh
1994年学术文章
@zh-cn
1994年学术文章
@zh-hans
1994年学术文章
@zh-my
1994年学术文章
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1994年學術文章
@yue
1994年學術文章
@zh-hant
name
Molecular characterization and ...... oxylate aminotransferase gene.
@en
Molecular characterization and ...... oxylate aminotransferase gene.
@nl
type
label
Molecular characterization and ...... oxylate aminotransferase gene.
@en
Molecular characterization and ...... oxylate aminotransferase gene.
@nl
prefLabel
Molecular characterization and ...... oxylate aminotransferase gene.
@en
Molecular characterization and ...... oxylate aminotransferase gene.
@nl
P2093
P2860
P356
P1433
P1476
Molecular characterization and ...... oxylate aminotransferase gene.
@en
P2093
P2860
P2888
P356
10.1007/BF02272842
P577
1994-07-01T00:00:00Z