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searching for Multiple sulfatase deficiency 5 found (19 total)

alternate case: multiple sulfatase deficiency

Arylsulfatase A (958 words) [view diff] exact match in snippet view article find links to article

metachromatic leukodystrophy, an autosomal recessive disease. Multiple sulfatase deficiency (MSD) is also associated with the ARSA gene. Arylsulfatase A

SUMF2 (817 words) [view diff] exact match in snippet view article find links to article

Newbold RF, Grompe M, Parenti G, Ballabio A (May 2003). "The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity

X-linked recessive chondrodysplasia punctata (931 words) [view diff] exact match in snippet view article find links to article

gamma-glutamyl carboxylase (GGCX), Xp contiguous deletion syndromes, and multiple sulfatase deficiency are all genetic conditions that are associated BCDP. This condition

Aldehyde tag (2,916 words) [view diff] case mismatch in snippet view article find links to article

, Ficner, R. and Rudolph, M. G. (2005) Molecular Basis for Multiple Sulfatase Deficiency and Mechanism for Formylglycine Generation of the Human

Radical SAM (6,094 words) [view diff] exact match in snippet view article find links to article

Borissenko LV, Peng J, Preusser A, Mariappan M, et al. (May 2003). "Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine