PHENYLKETONURIA DUE TO A DEFICIENCY OF DIHYDROPTERIDINE REDUCTASE

被引：300

作者：

KAUFMAN, S

HOLTZMAN, NA

MILSTIEN, S

BUTLER, IJ

KRUMHOLZ, A

机构：

[1] NIMH, LAB NEUROCHEM, BLDG 36, ROOM 3D-30, BETHESDA, MD 20014 USA

[2] JOHNS HOPKINS UNIV, SCH MED, DEPT PEDIAT, BALTIMORE, MD USA

[3] JOHNS HOPKINS UNIV, SCH MED, DEPT NEUROL, BALTIMORE, MD USA

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 1975年 / 293卷 / 16期

关键词：

D O I：

10.1056/NEJM197510162931601

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：785 / 790

页数：6

共 24 条

[1]

CRAINE JE, 1972, J BIOL CHEM, V247, P6082

[2] DETECTION OF HEPATIC PHENYLALANINE 4-HYDROXYLASE IN CLASSICAL PHENYLKETONURIA [J].

FRIEDMAN, PA ;

FISHER, DB ;

KANG, ES ;

KAUFMAN, S .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (02) :552-556

[3]

FRIEDMAN PA, 1972, J BIOL CHEM, V247, P4165

[4] NATURE OF MOLECULAR DEFECT IN PHENYLKETONURIA AND HYPERPHENYLALANINEMIA [J].

FRIEDMAN, PA ;

KAUFMAN, S ;

KANG, ES .

NATURE, 1972, 240 (5377) :157-&

[5]

FUTTERMAN S, 1957, J BIOL CHEM, V228, P1031

[6]

JERVIS GA, 1953, P SOC EXP BIOL MED, V82, P514

[7]

KANG ES, 1970, PEDIATRICS, V45, P83

[8]

KAUFMAN S, 1971, ADV ENZYMOL RAMB, V35, P245

[9] PHENYLALANINE HYDROXYLASE OF HUMAN LIVER - ASSAY AND SOME PROPERTIES [J].

KAUFMAN, S .

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1969, 134 (01) :249-&

[10]

KAUFMAN S, 1967, J BIOL CHEM, V242, P3934

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