EXPRESSION ANALYSIS OF MUTATION P244L, WHICH CAUSES MILD HYPERPHENYLALANINEMIA

被引：9

作者：

PEREZ, B ^{[1
]}

DESVIAT, LR ^{[1
]}

UGARTE, M ^{[1
]}

机构：

[1] UNIV AUTONOMA MADRID,CSIC,CTR BIOL MOLEC SEVERO OCHOA,E-28049 MADRID,SPAIN

来源：

HUMAN MUTATION | 1995年 / 5卷 / 02期

关键词：

D O I：

10.1002/humu.1380050217

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：188 / 190

页数：3

共 16 条

[1]

CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2

[2]

DAHL HHM, 1986, J BIOL CHEM, V261, P4148

[3]

DESVIAT LR, 1993, HUM GENET, V92, P254

[4]

DESVIAT LR, 1992, HUM MOL GENET, V9, P765

[5]

Eisensmith Randy C., 1992, Human Mutation, V1, P13, DOI 10.1002/humu.1380010104

[6]

GIBBS BS, 1993, J BIOL CHEM, V268, P8046

[7]

HARLOW E, 1988, ANTIBODIES LABORATOR

[8] LOCALIZATION OF COFACTOR BINDING-SITES WITH MONOCLONAL ANTIIDIOTYPE ANTIBODIES - PHENYLALANINE-HYDROXYLASE [J].

JENNINGS, IG ;

KEMP, BE ;

COTTON, RGH .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (13) :5734-5738

[9]

John Simon W. M., 1992, Human Mutation, V1, P147, DOI 10.1002/humu.1380010210

[10] HOMOLOGY BETWEEN PHENYLALANINE AND TYROSINE HYDROXYLASES REVEALS COMMON STRUCTURAL AND FUNCTIONAL DOMAINS [J].

LEDLEY, FD ;

DILELLA, AG ;

KWOK, SCM ;

WOO, SLC .

BIOCHEMISTRY, 1985, 24 (14) :3389-3394

← 1 2 →