HEREDITARY ERYTHROCYTE PYRUVATE-KINASE DEFICIENCY - MOLECULAR AND FUNCTIONAL STUDIES OF 4 MUTANT PK VARIANTS DETECTED IN SPAIN

被引：14

作者：

MARIE, J ^{[1
]}

VIVESCORRONS, JL ^{[1
]}

KAHN, A ^{[1
]}

KERNEMP, B ^{[1
]}

机构：

[1] HOSP CLIN & PROVINCIAL,POST GRAD HEMATOL SCH,BARCELONA,SPAIN

来源：

CLINICA CHIMICA ACTA | 1977年 / 81卷 / 02期

关键词：

D O I：

10.1016/0009-8981(77)90007-9

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：153 / 162

页数：10

共 26 条

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[2]

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HOFFBAUER, RW ;

BUSCH, D ;

ARNOLD, H ;

LOHR, GW .

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[4] ADDITIONAL DIAGNOSTIC PROCEDURES FOR DETECTION OF ABNORMAL RED-CELL PYRUVATE-KINASE [J].

BLUME, KG ;

ARNOLD, H ;

LOHR, GW ;

BEUTLER, E .

CLINICA CHIMICA ACTA, 1973, 43 (03) :443-446

[5]

BOIVIN P, 1972, PATHOL BIOL, V20, P583

[6]

BOIVIN P, 1972, NOUV REV FR HEMATOL, V12, P569

[7]

BOIVIN P, 1972, NOUV REV FR HEMATOL, V12, P159

[8]

BUCTEMKINE H, 1973, 7TH P INT S STRUCT F, P79

[9] ANOMALOUS GLYCOLYSIS IN HEMOLYTIC ANEMIA DUE TO PYRUVATE KINASE DEFICIENCY OF RED CELLS [J].

CARTIER, P ;

NAJMAN, A ;

LEROUX, JP ;

TEMKINE, H .

CLINICA CHIMICA ACTA, 1968, 22 (02) :165-&

[10]

CARTIER P, 1968, CR ACAD SCI D NAT, V266, P1680

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