Characterization of a Cys329Gly mutation causing hereditary factor VII deficiency

scientific article published on January 2006

Characterization of a Cys329Gly mutation causing hereditary factor VII deficiency is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1159/000093638
P698PubMed publication ID16914903

P2093author name stringFeng Chen
Fenghua Lan
Yushui Wu
Xiangdong Tu
Zhongyong Zhu
Yunzong Lian
P2860cites workNucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulationQ22254871
Nucleotide sequence of the gene for human factor IX (antihemophilic factor B)Q28646323
Gene for human factor X: a blood coagulation factor whose gene organization is essentially identical with that of factor IX and protein C.Q34190061
Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patientsQ40509506
Two novel mutations in severe factor VII deficiencyQ44937880
Two novel factor VII gene mutations in a Chinese family with factor VII deficiencyQ45872643
Molecular analysis of the genotype-phenotype relationship in factor VII deficiencyQ57263859
P433issue2
P304page(s)96-100
P577publication date2006-01-01
P1433published inActa HaematologicaQ15749687
P1476titleCharacterization of a Cys329Gly mutation causing hereditary factor VII deficiency
P478volume116