CONGENITAL DYSFIBRINOGENEMIAS - MOLECULAR ABNORMALITIES OF FIBRINOGEN

被引：7

作者：

MAMMEN, EF

机构：

[1] WAYNE STATE UNIV,COLL PHARM & ALLIED HLTH PROFESSIONS,DETROIT,MI 48202

[2] WAYNE STATE UNIV,SCH MED,DEPT PATHOL,DETROIT,MI 48202

[3] WAYNE STATE UNIV,SCH MED,DEPT PHYSIOL,DETROIT,MI 48202

来源：

BLUT | 1976年 / 33卷 / 04期

关键词：

D O I：

10.1007/BF00995218

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：229 / 234

页数：6

共 36 条

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SHAINOFF, JR ;

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[3] A NEW INHERITED COAGULATION DISORDER CAUSED BY AN ABNORMAL FIBRINOGEN (FIBRINOGEN BALTIMORE) [J].

BECK, EA ;

CHARACHE, P ;

JACKSON, DP .

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[4]

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

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BLOMBACK, B ;

MAMMEN, EF ;

PRASAD, AS .

NATURE, 1968, 218 (5137) :134-&

[6] FIBRINOGEN CLEVELAND-II - ABNORMAL FIBRINOGEN WITH DEFECTIVE RELEASE OF FIBRINOPEPTIDE-A [J].

CRUM, ED ;

SHAINOFF, JR ;

GRAHAM, RC ;

RATNOFF, OD .

JOURNAL OF CLINICAL INVESTIGATION, 1974, 53 (05) :1308-1319

[7]

FELTEN AV, 1965, SCHWEIZ MED WOCHSCHR, V95, P1453

[8]

FELTEN AV, 1969, BRIT J HAEMATOL, V16, P353

[9]

FORMAN WB, 1968, J LAB CLIN MED, V72, P455

[10]

FUNK C, 1970, EUR J CLIN INVEST, V1, P131

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