Genetic diagnosis of dysplasminogenemia: Detection of an Ala601-Thr mutation in 118 out of 125 families and identification of a mew Asp676-Asn mutation

Thrombosis and Haemostasis

Volumn 76, Issue 2, 1996, Pages 135-138

  Tsutsumi, Seiji ^a   Saito, Tetsuo ^a   Sakata, Toshiyuki ^b   Miyata, Toshiyuki ^b   Ichinose, Akitada ^a  

^a YAMAGATA UNIVERSITY   (Japan)

^b NATIONAL CEREBRAL AND CARDIOVASCULAR CENTER   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

PLASMINOGEN;

ARTICLE; DNA DETERMINATION; FAMILY STUDY; FEMALE; GENE MUTATION; GENETIC DISORDER; GENETICS; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PROTEIN DEFECT;

EID: 0029794495     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0038-1650541     Document Type: Article

References (17)

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