Article
Neutralizing Antibodies Against Adeno-Associated Viral Capsids in Patients with mut Methylmalonic Acidemia.
Human gene therapy - 1 May 2016
Harrington Elizabeth A, Sloan Jennifer L, Manoli Irini, Chandler Randy J, Schneider Mark, McGuire Peter J, Calcedo Roberto, Wilson James M, Venditti Charles P
Abstract excerpt
Isolated methylmalonic acidemia (MMA), a group of autosomal recessive inborn errors of metabolism, is most commonly caused by complete (mut(0)) or partial (mut(-)) deficiency of the enzyme methylmalonyl-CoA mutase (MUT). The severe metabolic instability and increased mortality experienced by many affected individuals, especially those with mut(0) MMA, has led centers to use elective liver transplantation as a...
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