Title : Sanfilippo syndrome type B, a lysosomal storage disease, is also a tauopathy.

Pub. Date : 2009 May 19

PMID : 19416848






1 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 The primary cause is mutation in the NAGLU gene, resulting in deficiency of alpha-N-acetylglucosaminidase and lysosomal accumulation of heparan sulfate. Heparitin Sulfate N-acetyl-alpha-glucosaminidase Homo sapiens