F8 mRNA studies in haemophilia A patients with different splice site mutations.
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Nonsense-mediated mRNA decay among coagulation factor genesGenetic testing in bleeding disordersAnalysis of F8 mRNA in haemophilia A patients with silent mutations or presumptive splice site mutations.Deep intronic 'mutations' cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNA.Deep intronic variations may cause mild hemophilia A.
P2860
F8 mRNA studies in haemophilia A patients with different splice site mutations.
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2010 nî lūn-bûn
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F8 mRNA studies in haemophilia A patients with different splice site mutations.
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F8 mRNA studies in haemophilia A patients with different splice site mutations.
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type
label
F8 mRNA studies in haemophilia A patients with different splice site mutations.
@en
F8 mRNA studies in haemophilia A patients with different splice site mutations.
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prefLabel
F8 mRNA studies in haemophilia A patients with different splice site mutations.
@en
F8 mRNA studies in haemophilia A patients with different splice site mutations.
@nl
P2093
P1433
P1476
F8 mRNA studies in haemophilia A patients with different splice site mutations.
@en
P2093
E Santagostino
F Rodeghiero
G Castaman
M E Mancuso
S H Giacomelli
P304
P356
10.1111/J.1365-2516.2010.02250.X
P577
2010-04-14T00:00:00Z