FIBRINOGEN NEW ORLEANS - HEREDITARY DYSFIBRINOGENEMIA WITH AN A-ALPHA CHAIN ABNORMALITY

被引：11

作者：

ANDES, WA ^{[1
]}

CHAVIN, SI ^{[1
]}

BELTRAN, G ^{[1
]}

STUCKEY, WJ ^{[1
]}

机构：

[1] OXFORD HAEMOPHILIA CTR, OXFORD, ENGLAND

来源：

THROMBOSIS RESEARCH | 1982年 / 25卷 / 1-2期

关键词：

D O I：

10.1016/0049-3848(82)90213-4

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：41 / 50

页数：10

共 23 条

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[2]

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[3]

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[4]

BELTRAN G, 1978, CLIN RES, V26, pA341

[5]

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[6] THROMBOGENESIS - FIBRINOGEN AND FIBRIN FORMATION [J].

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HOGG, DH ;

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[7]

BLOMBACK B, 1957, ARK KEMI, V10, P415

[8] FIBRINOGEN DETROIT - A MOLECULAR DEFECT IN N-TERMINAL DISULPHIDE KNOT OF HUMAN FIBRINOGEN [J].

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BLOMBACK, B ;

MAMMEN, EF ;

PRASAD, AS .

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[9]

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[10] PROTEIN SUBUNITS - TABLE [J].

DARNALL, DW ;

KLOTZ, IM .

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1972, 149 (01) :1-+

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