scholarly article | Q13442814 |
P356 | DOI | 10.1111/J.1365-2516.2006.01206.X |
P698 | PubMed publication ID | 16476093 |
P2093 | author name string | Hamaguchi M | |
Yamamoto K | |||
Okumura K | |||
Yamazaki T | |||
Naoe T | |||
Murate T | |||
Kojima T | |||
Takagi A | |||
Takamatsu J | |||
Matushita T | |||
Ikejiri M | |||
Yamakage N | |||
P2860 | cites work | Five novel mutations in the gene for human blood coagulation factor V associated with type I factor V deficiency | Q28204484 |
Quality control of mRNA function | Q34156109 | ||
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 mutations | Q47817298 | ||
Structure of the gene for human coagulation factor V | Q48176939 | ||
PARAHÆMOPHILIA | Q56029562 | ||
P433 | issue | 2 | |
P921 | main subject | heterozygosity | Q124059385 |
P304 | page(s) | 172-178 | |
P577 | publication date | 2006-03-01 | |
P1433 | published in | Haemophilia | Q15753375 |
P1476 | title | A case of coagulation factor V deficiency caused by compound heterozygous mutations in the factor V gene | |
P478 | volume | 12 |
Q45873732 | Combined 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 family | cites work | P2860 |
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