Orphanet Journal of Rare Diseases , Vol. 6, No. 1. , 72, doi:10.1186/1750-1172-6-72 :Mucopolysaccharidosis type II is a rare, life-limiting, X-linked recessive disease characterised by deficiency of the lysosomal enzyme iduronate-2-sulfatase.
http://www.citeulike.org/user/ajaymalik/article/10000090
http://www.citeulike.org/user/ajaymalik/article/10000090
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