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Vivienne M Homer

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Thrombosis and Haemostasis|September 28, 2002
Novel fibrinogen truncation with deletion of Bbeta chain residues 440-461 causes hypofibrinogenaemiaVivienne M Homer, Stephen O Brennan, Paul Ockelford, et al.
Human Mutation|October 15, 2008
A deep intronic mutation in FGB creates a consensus exonic splicing enhancer motif that results in afibrinogenemia caused by aberrant mRNA splicing, which can be corrected in vitro with antisense oligonucleotide treatmentRyan L Davis, Vivienne M Homer, Peter M George, et al.
Annals of Neurology|June 29, 2005
Mental retardation and ataxia due to normotriglyceridemic hypobetalipoproteinemiaVivienne M Homer, Peter M George, Stephen du Toit, et al.
Atherosclerosis|September 4, 2007
Identification and characterization of two non-secreted PCSK9 mutants associated with familial hypercholesterolemia in cohorts from New Zealand and South AfricaVivienne M Homer, A David Marais, Francesca Charlton, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Thrombosis and Haemostasis|September 28, 2002
Novel fibrinogen truncation with deletion of Bbeta chain residues 440-461 causes hypofibrinogenaemiaVivienne M Homer, Stephen O Brennan, Paul Ockelford, et al.
Human Mutation|October 15, 2008
A deep intronic mutation in FGB creates a consensus exonic splicing enhancer motif that results in afibrinogenemia caused by aberrant mRNA splicing, which can be corrected in vitro with antisense oligonucleotide treatmentRyan L Davis, Vivienne M Homer, Peter M George, et al.
Annals of Neurology|June 29, 2005
Mental retardation and ataxia due to normotriglyceridemic hypobetalipoproteinemiaVivienne M Homer, Peter M George, Stephen du Toit, et al.
Atherosclerosis|September 4, 2007
Identification and characterization of two non-secreted PCSK9 mutants associated with familial hypercholesterolemia in cohorts from New Zealand and South AfricaVivienne M Homer, A David Marais, Francesca Charlton, et al.
Pageof 1