Hematologically important mutations: Triosephosphate isomerase

被引：16

作者：

Schneider, A ^{[1
]}

CohenSolal, M ^{[1
]}

机构：

[1] HOP HENRI MONDOR,INSERM,U91,UNITE RECH GENET MOL & HEMATOL,F-94010 CRETEIL,FRANCE

来源：

BLOOD CELLS MOLECULES AND DISEASES | 1996年 / 22卷 / 06期

关键词：

D O I：

10.1006/bcmd.1996.0011

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：82 / 84

页数：3

共 14 条

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[2]

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[3]

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[4]

COHENSOLAL M, 1996, UNPUB

[5]

COHENSOLAL M, 1966, UNPUB

[6] PREMATURE TRANSLATION TERMINATION MEDIATES TRIOSEPHOSPHATE ISOMERASE MESSENGER-RNA DEGRADATION [J].

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[7] HUMAN TRIOSE-PHOSPHATE ISOMERASE DEFICIENCY - A SINGLE AMINO-ACID SUBSTITUTION RESULTS IN A THERMOLABILE ENZYME [J].

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NEUBAUER RA, 1992, EUR J PEDIATR, V151, P232

[9] HUMAN TRIOSEPHOSPHATE ISOMERASE - SUBSTITUTION OF ARG FOR GLY AT POSITION 122 IN A THERMOLABILE ELECTROMORPH VARIANT, TPI-MANCHESTER [J].

PERRY, BA ;

MOHRENWEISER, HW .

HUMAN GENETICS, 1992, 88 (06) :634-638

[10] TRIOSEPHOSPHATE ISOMERASE DEFICIENCY - REPETITIVE OCCURRENCE OF POINT MUTATION IN AMINO-ACID-104 IN MULTIPLE APPARENTLY UNRELATED FAMILIES [J].

SCHNEIDER, A ;

WESTWOOD, B ;

YIM, C ;

PRCHAL, J ;

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WARRIER, R ;

BEUTLER, E .

AMERICAN JOURNAL OF HEMATOLOGY, 1995, 50 (04) :263-268

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