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A New Key To Fight Rare Childhood Disease
Published February 3, 2010, 5:34 am, Medical News Today
A research team led by biochemist Scott Garman at the University of Massachusetts Amherst has for the first time determined the mechanism of one of the cell's "recycling" enzymes, human alpha-galactosidase or alpha-GAL, as it breaks down substances in the lysosome, the cell's recycling center. The work promises to aid treatment of a rare childhood metabolic disorder, Fabry disease. Patients may ...
Research offers new hope for rare metabolic disorder
Published February 2, 2010, 8:51 pm, News-Medical-Net
A research team led by biochemist Scott Garman at the University of Massachusetts Amherst has for the first time determined the mechanism of one of the cell's "recycling" enzymes, human alpha-galactosidase or alpha-GAL, as it breaks down substances in the lysosome, the cell's recycling center.
Biochemists Provide New Key for Treating Fabry Disease, a Rare Childhood Disorder
Published February 2, 2010, 1:42 pm, PhysOrg
(PhysOrg.com) -- A research team led by biochemist Scott Garman at the University of Massachusetts Amherst has for the first time determined the mechanism of one of the cell`s 'recycling' enzymes, human alpha-galactosidase or alpha-GAL, as it breaks down substances in the lysosome, the cell's recycling center. The work promises to aid treatment of a rare childhood metabolic disorder, Fabry ...
A New Key to Fight Rare Childhood Disease
Published February 2, 2010, 8:35 am, Newswise
Biochemists led by Scott Garman have for the first time determined the mechanism of one of the cell's "recycling" enzymes, human alpha-GAL, as it breaks down substances in the lysosome, the cell's recycling center. It promises to aid treatment of a rare childhood metabolic disorder, Fabry disease.
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