Hematologically important mutations: Red cell pyruvate kinase

被引：12

作者：

Baronciani, L ^{[1
]}

Bianchi, P ^{[1
]}

Zanella, A ^{[1
]}

机构：

[1] OSPED MAGGIORE,IRCCS,CTR TRASFUS & IMMUNOL TRAPIANTI,I-20122 MILAN,ITALY

来源：

BLOOD CELLS MOLECULES AND DISEASES | 1996年 / 22卷 / 21期

关键词：

D O I：

10.1006/bcmd.1996.0107

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：259 / 264

页数：6

共 36 条

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BEUTLER, E .

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[2] MOLECULAR STUDY OF PYRUVATE-KINASE DEFICIENT PATIENTS WITH HEREDITARY NONSPHEROCYTIC HEMOLYTIC-ANEMIA [J].

BARONCIANI, L ;

BEUTLER, E .

JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (04) :1702-1709

[3] STUDY OF THE MOLECULAR DEFECTS IN PYRUVATE-KINASE DEFICIENT PATIENTS AFFECTED BY NONSPHEROCYTIC HEMOLYTIC-ANEMIA [J].

BARONCIANI, L ;

MAGALHAES, LQ ;

MAHONEY, DH ;

WESTWOOD, B ;

ADEKILE, AD ;

LAPPIN, TRJ ;

BEUTLER, E .

BLOOD CELLS MOLECULES AND DISEASES, 1995, 21 (01) :49-55

[4]

BARONCIANI L, 1995, CLIN RES, V43, pA341

[5]

Beutler E, 1996, HUM MUTAT, V7, P1

[6]

Bianchi P., 1995, Blood, V86, p133A

[7]

BIANCHI P, 1994, BLOOD, V84, pA14

[8]

BIANCHI P, 1996, IN PRESS BLOOD S1, V88

[9]

Fujii H., 1995, Blood, V86, p133A

[10]

Huppke P., 1996, UNPUB

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