FACTOR-XIII DEFICIENCY - GENETIC STUDY OF 2 AFFECTED KINDREDS IN FINLAND

被引：18

作者：

MCDONAGH, J

MCDONAGH, RP

MYLLYLA, G

IKKALA, E

机构：

[1] UNIV N CAROLINA,SCH MED,THROMBOSIS RES CTR,CHAPEL HILL,NC 27514

[2] FINNISH RED CROSS,BLOOD TRANSF SERV,HELSINKI,FINLAND

来源：

BLOOD | 1974年 / 43卷 / 03期

关键词：

D O I：

10.1182/blood.V43.3.327.327

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：327 / 332

页数：6

共 18 条

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[2] PLASMA TRANSGLUTAMINASE ACTIVITY IN CONGENITAL TOTAL AND PARTIAL FACTOR-XIII DEFICIENCY - PROBLEMATICS OF FACTOR-XIII DETERMINATION [J].

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EGLI, H .

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RAE, BA .

AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE, 1971, 1 (02) :174-+

[4]

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[5]

Ikkala E, 1968, Thromb Diath Haemorrh Suppl, V28, P13

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[7]

IKKALA EERO, 1964, SCAND J HAEMATOL, V1, P308

[8] DIAGNOSTIC AND GENETIC STUDIES ON FIBRIN-STABILIZING FACTOR WITH A NEW ASSAY BASED ON AMINE E INCORPORATION [J].

LORAND, L ;

URAYAMA, T ;

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JOURNAL OF CLINICAL INVESTIGATION, 1969, 48 (06) :1054-&

[9]

LORAND L, 1970, AM J HUM GENET, V22, P89

[10] TRANSPEPTIDASE SYSTEM WHICH CROSSLINKS FIBRIN BY GAMMA-GLUTAMYL-EPSILON-LYSINE BONDS [J].

LORAND, L ;

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BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1968, 31 (02) :222-&

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