A case of coagulation factor V deficiency caused by compound heterozygous mutations in the factor V gene

scientific article published in March 2006

A case of coagulation factor V deficiency caused by compound heterozygous mutations in the factor V gene is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1111/J.1365-2516.2006.01206.X
P698PubMed publication ID16476093

P2093author name stringHamaguchi M
Yamamoto K
Okumura K
Yamazaki T
Naoe T
Murate T
Kojima T
Takagi A
Takamatsu J
Matushita T
Ikejiri M
Yamakage N
P2860cites workFive novel mutations in the gene for human blood coagulation factor V associated with type I factor V deficiencyQ28204484
Quality control of mRNA functionQ34156109
Inherited defects of coagulation factor V: the hemorrhagic side.Q36367017
Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V: Broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutationsQ47817298
Structure of the gene for human coagulation factor VQ48176939
PARAHÆMOPHILIAQ56029562
P433issue2
P921main subjectheterozygosityQ124059385
P304page(s)172-178
P577publication date2006-03-01
P1433published inHaemophiliaQ15753375
P1476titleA case of coagulation factor V deficiency caused by compound heterozygous mutations in the factor V gene
P478volume12

Reverse relations

Q45873732Combined deficiency of factors V and VIII by chance coinheritance of parahaemophilia and haemophilia A, but not by mutations of either LMAN1 or MCFD2, in a Japanese familycites workP2860

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