Thirty-three novel mutations in the protein C gene

Thrombosis and Haemostasis

Volumn 83, Issue 1, 2000, Pages 86-92

  Alhenc Gelas, Martine ^a   Gandrille, Sophie ^a   Aubry, Marie Laurence ^a   Aiach, Martine ^a   Abgrall, J F ^b   Aillaud, M F ^c   Juhan Vague, I ^c   Ajzenberg, N ^d   Dreyfus, M ^d   Berruyer, M ^e   Trzeciak, M C ^e   Boinot, C ^f   Bridey, F ^g   De Prost, D ^g   Brun, S ^h   David, M ⁱ   De Maistre, E ^aa   Lecompte, T ^aa   De Moerloose, P ^j   Reber, G ^j   Denninger, M H ^k   Dupuy, E ^l   Emmerich, J ^a   Fiessinger, J N ^a   Jaque, A ^a   Rance, A ^a   Sirieix, M E ^a   Vitoux, J F ^a   Gouault Heilmann, M ^m   Jude, B ⁿ   Le Querrec, A ^o   Mexme, M ^aa   Michaud Mallet, A ^p   Nowak Gottl, U ^q   Priollet, P ^r   Reynaud, J ^s   Siguret, V ^t   Tardy, B ^u   Toulon, P ^v   Toumi, N H ^w   Truchaud, F ^x   Vergnes, C ^y   Wolf, M ^z   more..

^a HÔPITAL BROUSSAIS   (France)

^b CHU MORVAN   (France)

^c TIMONE HOSPITAL   (France)

^d BICÊTRE HOSPITAL   (France)

^e EDOUARD HERRIOT HOSPITAL   (France)

^f POITIERS UNIVERSITY HOSPITAL   (France)

^g BICHAT HOSPITAL   (France)

^h Hopital Gaston Doumergue   (France)

ⁱ UNIVERSITY OF MONTREAL   (Canada)

^j GENEVA UNIVERSITY HOSPITALS   (Switzerland)

^k BEAUJON HOSPITAL   (France)

^l HÔPITAL LARIBOISIÈRE   (France)

^m HENRI MONDOR HOSPITAL   (France)

ⁿ LILLE UNIVERSITY HOSPITAL   (France)

^o CHU CÔTE DE NACRE   (France)

^p INSTITUT ARNAULT TZANCK   (France)

^q UNIVERSITY OF MÜNSTER   (Germany)

^r SAINT JOSEPH HOSPITAL   (France)

^s HÔPITAL NORD   (France)

^t HÔPITAL CHARLES FOIX   (France)

^u SERVICE DE NEUROLOGIE   (France)

^v Hôpital Bellevue ^*  (France)

^w CHILDREN S HOSPITAL   (Tunisia)

^x INSTITUT DE BIOLOGIE   (France)

^y HAUT LÉVÊQUE HOSPITAL   (France)

^z HÔPITAL ANTOINE BÉCLÈRE   (France)

^aa Hop Antoine Béclère ^*

more..

Author keywords

Coagulation; Gene; Protein C; Thrombosis

Indexed keywords

AMINO ACID; PROTEIN C;

ADULT; ARTICLE; DENATURING GRADIENT GEL ELECTROPHORESIS; FEMALE; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; GENETIC POLYMORPHISM; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PROTEIN C DEFICIENCY; SCREENING;

EID: 0033983871     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1613762     Document Type: Article

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