-
Sanfilippo syndrome, also
known as
mucopolysaccharidosis type III (MPS III), is a rare
autosomal recessive lysosomal storage disease that
primarily affects...
- 000-1:150,000
males MPS IIIA
Sanfilippo syndrome A
Sulfamidase deficiency 252900 SGSH 17q25.3
Heparan sulfamidase Heparan sulfate Developmental delay, severe...
- S2CID 25869397. "Entrez Gene: SGSH N-sulfoglucosamine
sulfohydrolase (
sulfamidase)".
Esposito S,
Balzano N,
Daniele A,
Villani GR,
Perkins K,
Weber B,...
-
common use
include cyclamate sulfamatase,
cyclamate sulfamidase, and
cyclohexylsulfamate sulfamidase. This
enzyme parti****tes in
caprolactam degradation...
- der
Horst syndrome Henoch–Schönlein
purpura Hepadnovirus D
Heparane sulfamidase deficiency Heparin-induced
thrombopenia Hepatic cystic hamartoma Hepatic...
-
range of
enzymes such as lyases, glucuronidases, sulfoesterases, and
sulfamidases. The
lyases have
mainly been used in heparin/HS studies. The bacterium...
- sulfohydrolase.
Other names in
common use
include sulfoglucosamine sulfamidase,
heparin sulfamidase, 2-desoxy-D-glucoside-2-sulphamate
sulphohydrolase (sulphamate...
