Add to ORKGBibliography: p. 184-215.xvii, 215, [122] p., [21] leaves of plates : ill. ; 30 cm.Aims to clone the gene for [alpha]-L-iduronidase, to enable molecular genetic diagnosis of mutations causing Mucopolysaccharidosis type I for more accurate disease prognosis, and make possible new therapy protocols such as enzyme replacement therapy and gene replacement therapy.Thesis (Ph.D.)--University of Adelaide, Dept. of Pathology, 199
Mucopolysaccharidosis type I (MPS-I) is an autosomal recessive lysosomal storage disorder resulting ...
Abstract Background Mucopolysaccharidosis type I (MPS I) is an autosomal recessive disease due to de...
The mucopolysaccharidoses (MPS) are a group of lysosomal storage disorders in which the storage mate...
Mucopolysaccharidosis type I (MPS-I) is an autosomal recessive disease caused by mutations in the al...
Mucopolysaccharidosis type I (MPS I) is an autosomal recessive lysosomal storage disorder caused by ...
Mucopolysaccharidosis type I (MPSI) is a rare autosomal recessive disorder caused by mutations in th...
Bibliography: p. 252-281.xiii, 281, [110] p., [11] leaves of plates : ill. ; 35 cm.Identifies and an...
In this study we have investigated a group of 29 Brazilian patients, who had been diagnosed with the...
[[abstract]]α-L-Iduroindase (IDUA) is one of the lysosomal enzymes involved in metabolic degradation...
Mutational analysis of the IDUA gene was performed in a cohort of 102 European patients with mucopol...
University of Minnesota Ph.D. dissertation. November 2010. Major: Molecular, Cellular, Developmental...
Mucopolysaccharidosis type I (MPS I) is an autosomal recessive genetic disorder resulting from defic...
Mucopolysaccharidosis type I (MPS I) is a rare inherited metabolic disorder caused by defects in alp...
p.589-604Mucopolysaccharidoses (MPS) are rare genetic diseases caused by the deficiency of one of th...
Mucopolysaccharidosis I (McKusick 25280, Hurler syndrome, Scheie syndrome) is caused by a deficiency...
Mucopolysaccharidosis type I (MPS-I) is an autosomal recessive lysosomal storage disorder resulting ...
Abstract Background Mucopolysaccharidosis type I (MPS I) is an autosomal recessive disease due to de...
The mucopolysaccharidoses (MPS) are a group of lysosomal storage disorders in which the storage mate...
Mucopolysaccharidosis type I (MPS-I) is an autosomal recessive disease caused by mutations in the al...
Mucopolysaccharidosis type I (MPS I) is an autosomal recessive lysosomal storage disorder caused by ...
Mucopolysaccharidosis type I (MPSI) is a rare autosomal recessive disorder caused by mutations in th...
Bibliography: p. 252-281.xiii, 281, [110] p., [11] leaves of plates : ill. ; 35 cm.Identifies and an...
In this study we have investigated a group of 29 Brazilian patients, who had been diagnosed with the...
[[abstract]]α-L-Iduroindase (IDUA) is one of the lysosomal enzymes involved in metabolic degradation...
Mutational analysis of the IDUA gene was performed in a cohort of 102 European patients with mucopol...
University of Minnesota Ph.D. dissertation. November 2010. Major: Molecular, Cellular, Developmental...
Mucopolysaccharidosis type I (MPS I) is an autosomal recessive genetic disorder resulting from defic...
Mucopolysaccharidosis type I (MPS I) is a rare inherited metabolic disorder caused by defects in alp...
p.589-604Mucopolysaccharidoses (MPS) are rare genetic diseases caused by the deficiency of one of th...
Mucopolysaccharidosis I (McKusick 25280, Hurler syndrome, Scheie syndrome) is caused by a deficiency...
Mucopolysaccharidosis type I (MPS-I) is an autosomal recessive lysosomal storage disorder resulting ...
Abstract Background Mucopolysaccharidosis type I (MPS I) is an autosomal recessive disease due to de...
The mucopolysaccharidoses (MPS) are a group of lysosomal storage disorders in which the storage mate...