<p>* DS: Dermatan sulfate, HS: Heparan sulfate, CS: Chondroitin sulfate, KS: Keratan sulfate, GAGs: glycosaminoglycans.</p><p>The mucopolysaccharidoses and mucolipidosis II and III.</p
The mucopolysaccharidoses (MPSs) are a group of rare lysosomal storage disorders caused by deficienc...
Mucopolysaccharidosis type III (MPS III), or Sanfilippo syndrome, is a lysosomal storage disease in ...
The article is devoted to one of the hereditary diseases — mucopolysaccharidosis type II, which is ...
Ms received 12.07.04 Accepted 14.10.04 Summary: The mucopolysaccharidoses (MPS) is characterized by ...
The mucopolysaccharidoses are a family of genetic diseases involving faulty degradation of one or mo...
The catabolism of glycosaminoglycans begins with endo-hydrolysis of polysaccharides to oligosacchari...
The mucopolysaccharidoses (MPS) are a family of lyso-somal storage diseases caused by enzyme deficie...
Mucopolysaccharidosis (MPS) type I and II are two closely related lysosomal storage diseases associa...
Heparan sulfate (HS) catabolism begins with endo-degradation of the polysaccharide to smaller HS oli...
The catabolism of glycosaminoglycans begins with endohydrolysis of polysaccharides to oligosaccharid...
Heparan sulfate (HS) catabolism begins with endo-degradation of the polysaccharide to smaller HS oli...
Sulfated glycosaminoglycans (heparan sulfate, chondroitin sulfate, dermatan sulfate, and keratan su...
Mucopolysaccharidosis IIID (MPS IIID) is one of the rarest of the MPS-III syndromes. To date, the cl...
There are six readily distinguishable forms of mucopolysaccharidoses. The disorders each result from...
Mucopolysaccharidosis type IIIA (MPS IIIA, Sanfilippo A) is a neurodegenerative lysosomal storage di...
The mucopolysaccharidoses (MPSs) are a group of rare lysosomal storage disorders caused by deficienc...
Mucopolysaccharidosis type III (MPS III), or Sanfilippo syndrome, is a lysosomal storage disease in ...
The article is devoted to one of the hereditary diseases — mucopolysaccharidosis type II, which is ...
Ms received 12.07.04 Accepted 14.10.04 Summary: The mucopolysaccharidoses (MPS) is characterized by ...
The mucopolysaccharidoses are a family of genetic diseases involving faulty degradation of one or mo...
The catabolism of glycosaminoglycans begins with endo-hydrolysis of polysaccharides to oligosacchari...
The mucopolysaccharidoses (MPS) are a family of lyso-somal storage diseases caused by enzyme deficie...
Mucopolysaccharidosis (MPS) type I and II are two closely related lysosomal storage diseases associa...
Heparan sulfate (HS) catabolism begins with endo-degradation of the polysaccharide to smaller HS oli...
The catabolism of glycosaminoglycans begins with endohydrolysis of polysaccharides to oligosaccharid...
Heparan sulfate (HS) catabolism begins with endo-degradation of the polysaccharide to smaller HS oli...
Sulfated glycosaminoglycans (heparan sulfate, chondroitin sulfate, dermatan sulfate, and keratan su...
Mucopolysaccharidosis IIID (MPS IIID) is one of the rarest of the MPS-III syndromes. To date, the cl...
There are six readily distinguishable forms of mucopolysaccharidoses. The disorders each result from...
Mucopolysaccharidosis type IIIA (MPS IIIA, Sanfilippo A) is a neurodegenerative lysosomal storage di...
The mucopolysaccharidoses (MPSs) are a group of rare lysosomal storage disorders caused by deficienc...
Mucopolysaccharidosis type III (MPS III), or Sanfilippo syndrome, is a lysosomal storage disease in ...
The article is devoted to one of the hereditary diseases — mucopolysaccharidosis type II, which is ...