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pro vyhledávání: '"Hemophilia A/complications/ethnology/ genetics"'
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency
Autor:
Stylianos E. Antonarakis, William C. Nichols, David Ginsburg, Flora Peyvandi, Colette Rossier, Marguerite Neerman-Arbez, Edward G. D. Tuddenham, John H. McVey, Michael A. Morris, K. M. Johnson
Publikováno v:
Blood, Vol. 93, No 7 (1999) pp. 2253-2260
Scopus-Elsevier
Europe PubMed Central
Scopus-Elsevier
Europe PubMed Central
Combined factor V-factor VIII deficiency (F5F8D) is a rare, autosomal recessive coagulation disorder in which the levels of both coagulation factors V and VIII are diminished. The F5F8D locus was previously mapped to a 1-cM interval on chromosome 18q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16c1c485619af3e5647de915aea55fda
https://archive-ouverte.unige.ch/unige:8935
https://archive-ouverte.unige.ch/unige:8935
