Michael A Morris Selected Research

Afibrinogenemia (Fibrinogen Deficiency)

12/2004	Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells.
12/2003	Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion.
05/2003	Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family.

3	Afibrinogenemia (Fibrinogen Deficiency) 12/2004 - 05/2003
1	Hemophilia A (Haemophilia) 05/2006
1	Myoclonic Epilepsies (Myoclonic Encephalopathy) 11/2003

2	Nonsense Codon (Nonsense Mutation)IBA 12/2004 - 05/2003
1	Factor V (Coagulation Factor V)IBA 05/2006
1	RNA (Ribonucleic Acid)IBA 12/2004
1	Fibrinogen (Factor I)IBA 12/2003
1	DNA (Deoxyribonucleic Acid)IBA 11/2003