Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to Thr

Journal article

Peer reviewed

S Kemahli, M ALHENC-GELAS, S Gandrille, M Aiach, N Akar and S Cin

Blood coagulation & fibrinolysis, Vol.9(4), pp.351-354

06/1998

PMID: 9690806

Abstract

Biological and medical sciences

Hematologic and hematopoietic diseases

Medical sciences

Platelet diseases and coagulopathies

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Title: Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to Thr
Creators - without role: S Kemahli - Ankara University
M ALHENC-GELAS - Haemostasis Laboratory, Broussais Hospital, Paris, France
S Gandrille - Haemostasis Laboratory, Broussais Hospital, Paris, France
M Aiach - Haemostasis Laboratory, Broussais Hospital, Paris, France
N Akar - Ankara University
S Cin - Ankara University
Publication Details: Blood coagulation & fibrinolysis, Vol.9(4), pp.351-354
Publisher: The Scientist
Identifiers: 9913368308331
Academic Unit: Alfaisal University
Language: English
Resource Type: Journal article