A splicing donor site point mutation in intron 6 of the plasmin inhibitor (alpha2 antiplasmin) gene with heterozygous deficiency and a bleeding tendency.

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Bibliographic Details
Title: A splicing donor site point mutation in intron 6 of the plasmin inhibitor (alpha2 antiplasmin) gene with heterozygous deficiency and a bleeding tendency.
Authors: Hanss MM; Haematology Laboratory, L Pradel Hospital, Lyon, France. michel.hanss@chu-lyon.fr, Farcis M, Ffrench PO, de Mazancourt P, Dechavanne M
Source: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis [Blood Coagul Fibrinolysis] 2003 Jan; Vol. 14 (1), pp. 107-11.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Lippincott Williams And Wilkins Country of Publication: England NLM ID: 9102551 Publication Model: Print Cited Medium: Print ISSN: 0957-5235 (Print) Linking ISSN: 09575235 NLM ISO Abbreviation: Blood Coagul Fibrinolysis Subsets: MEDLINE
Database: MEDLINE Ultimate
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