DEFICIENCY OF TYROSINE-HYDROXYLASE OR TRYPTOPHAN-HYDROXYLASE - A POSSIBLE CAUSE OF 2 HYPOTHETICAL METABOLIC DISEASES

被引：6

作者：

BARTHOLOME, K

机构：

来源：

ACTA PAEDIATRICA SCANDINAVICA | 1983年 / 72卷 / 06期

关键词：

D O I：

10.1111/j.1651-2227.1983.tb09842.x

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：921 / 922

页数：2

共 8 条

[1] BARTHOLOME K, 1974, LANCET, V2, P1580
[2] BARTHOLOME K, 1975, LANCET, V2, P1042
[3] BARTHOLOME K, 1977, PEDIATRICS, V59, P757
[4] FRIEDMAN PA, 1972, J BIOL CHEM, V247, P4165
[5] Kaufman S., 1974, MOL MECHANISMS OXYGE, P285
[6] REY F, 1976, NEW ENGL J MED, V295, P1138
[7] SHIMAN R, 1971, J BIOL CHEM, V246, P1330
[8] NEW VARIANT OF PHENYLKETONURIA WITH PROGRESSIVE NEUROLOGICAL ILLNESS UNRESPONSIVE TO PHENYLALANINE RESTRICTION
SMITH, I
CLAYTON, BE
WOLFF, OH
[J]. LANCET, 1975, 1 (7916) : 1108 - 1111