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Vijyalakshmi IB
Publications
Dysostosis Multiplex (Gm-1 Gangliosidosis: Type II)
GM1 gangliosidosis is an autosomal recessive lysosomal storage disorder characterized by the generalized accumulation of GM1 ganglioside, oligosaccharides, and the mucopolysaccharide keratan sulfate (and their derivatives). Deficiency of the lysosomal hydrolase, acid β -galactosidase, causes GM1 gangliosidosis. GM1 gangliosidosis is a rare dis... Read More»
Madhu KJ, Vijyalakshmi IB, Chitra Narsimhan and CN Manjunath
Case Report: Cardiovasc Ther 2016, 1: 102
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