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ACID MALTASE DEFICIENCY--GENE ENZYME REPLACEMENT THERAPY

$0M01FY2000RRNIH

New York University School Of Medicine, New York NY

Investigators

Linked publications & trials

Abstract

Genetic defeciency of lysosomal acid alpha glucosidase or acid maltase (GAA) results in acid maltase deficiency or glycogen storage disease type II (GSDII).The investigator has administered a vector that contains the gene for human acid maltase for gene replacement therapy in a cow model and would like to administer the gene to the mouse model. This is a lab only study to investigate tissues collected at sacrifice for gene expression. The Core Laboratory was utilized for DNA Isolation, DNA sequencing (manual), oligonucleotide synthesis, and Recombinant DNA techniques.

View original record on NIH RePORTER →