GENETICS AND PATHOGENESIS OF HUMAN UROPORPHYRINOGEN DECARBOXYLASE DEFECTS

被引：45

作者：

ELDER, GH ^{[1
]}

ROBERTS, AG ^{[1
]}

DESALAMANCA, RE ^{[1
]}

机构：

[1] HOSP CLIN SAN CARLOS,DEPT INTERNAL MED,MADRID,SPAIN

来源：

CLINICAL BIOCHEMISTRY | 1989年 / 22卷 / 03期

关键词：

D O I：

10.1016/S0009-9120(89)80072-4

中图分类号：

R446 [实验室诊断]; R-33 [实验医学、医学实验];

学科分类号：

1001 ;

摘要：

引用

页码：163 / 168

页数：6

共 34 条

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[9] HEREDITARY AND NON-HEREDITARY FORM OF CHRONIC HEPATIC PORPHYRIA - DIFFERENT BEHAVIOR OF UROPORPHYRINOGEN DECARBOXYLASE IN LIVER AND ERYTHROCYTES [J].

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[10]

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