Search Results - "Pinto, Louise Lapagesse Carmargo"
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Enzyme replacement therapy for mucopolysaccharidoses I, II and VI: recommendations from a group of Brazilian F experts
Published in Revista da Associacao Medica Brasileira (1992) (01-05-2010)“…Mucopolysaccharidoses (MPS) are rare genetic diseases caused by deficiency of specific lysosomal enzymes that affect catabolism of glycosaminoglycans (GAG)…”
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