Molecular analysis of iduronate -2- sulfatase gene in Tunisian patients with mucopolysaccharidosis type II

Clinical and Molecular Characterization of Patients with Mucopolysaccharidosis Type I in an Algerian Series

Mucopolysaccharidoses (MPS’s) represent a subgroup of lysosomal storage diseases related to a defici

Mucopolysaccharidosis Type II: A Kenyan Case Series

Hunter syndrome, or mucopolysaccharidosis type 2 (MPS2), is a lysosomal storage disorder associated

Clinical, biochemical, and molecular characterization of mucopolysaccharidosis type <scp>III</scp> in 34 <scp>Egyptian</scp> patients

Abstract Mucopolysaccharidosis type III (MPS III) is a rare autosomal recessive lysosomal storage d

Challenges and Opportunities with Providing Genetic Testing and Counseling for Mucopolysaccharidosis Type II in Kenya

Abstract Limited or absent genetic counseling and testing resources in low- and medium-inc

The G1057D polymorphism of IRS-2 gene is not associated with type 2 diabetes and obese patients among ethnic groups in Tunisian population

Transcription factor-7-like 2 gene variants are strongly associated with type 2 diabetes in Tunisian Arab subjects