Ala601-Thr type dysplasminogenaemia genetically diagnosed in patients with retinochoroidal vascular disorders

British Journal of Haematology

Volumn 99, Issue 2, 1997, Pages 301-303

  Murata, Masatoshi ^a   Ooe, Asako ^a   Izumi, Tomonori ^a   Nakagawa, Michihiro ^a   Takahashi, Shigeki ^a   Ishikawa, Masaaki ^b   Mori, Kazuo ^b   Ichinose, Akitada ^a  

^a YAMAGATA UNIVERSITY   (Japan)

^b TOHOKU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Circulatory disturbances; Dysplasminogenaemia; Genetic diagnosis; Small vessels; Thrombosis

Indexed keywords

ALANINE; PLASMINOGEN; THREONINE;

ADULT; AGED; ARTICLE; CASE REPORT; CENTRAL RETINA ARTERY OCCLUSION; CENTRAL RETINA VEIN OCCLUSION; CHORIORETINOPATHY; DNA DETERMINATION; FEMALE; FIBRINOLYSIS; GENE MUTATION; HUMAN; ISCHEMIC OPTIC NEUROPATHY; MALE; PLASMINOGEN DEFICIENCY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; THROMBOSIS; VASCULAR DISEASE;

EID: 0030701948     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1997.4103229.x     Document Type: Article

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