FAMILY STUDIES ON ACTIVITY OF UROPORPHYRINOGENI SYNTHASE IN DIAGNOSIS OF ACUTE INTERMITTENT PORPHYRIA

被引：20

作者：

ASTRUP, EG

机构：

来源：

CLINICAL SCIENCE AND MOLECULAR MEDICINE | 1978年 / 54卷 / 03期

关键词：

D O I：

10.1042/cs0540251

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：251 / 256

页数：6

共 24 条

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GRANICK, S ;

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LEVERE, RD ;

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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1972, 69 (09) :2381-&

[4]

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[5]

Kappas A, 1974, Res Publ Assoc Res Nerv Ment Dis, V53, P225

[6]

KOEHL C, 1975, NOUV PRESSE MED, V4, P2735

[7]

MAUZERALL D, 1956, J BIOL CHEM, V219, P435

[8] INTERMITTENT ACUTE PORPHYRIA - DEMONSTRATION OF A GENETIC DEFECT IN PORPHOBILINOGEN METABOLISM [J].

MEYER, UA ;

MARVER, HS ;

STRAND, LJ ;

REES, AC ;

DOSS, M .

NEW ENGLAND JOURNAL OF MEDICINE, 1972, 286 (24) :1277-&

[9]

MEYER UA, 1973, FED PROC, V32, P1649

[10] INTERMITTENT ACUTE PORPHYRIA - CLINICAL AND BIOCHEMICAL STUDIES OF DISORDERED HEME BIOSYNTHESIS [J].

MEYER, UA .

ENZYME, 1973, 16 (1-6) :334-342

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