Title : The videofluoroscopic swallowing study shows a sustained improvement of dysphagia in children with Niemann-Pick disease type C after therapy with miglustat.

Pub. Date : 2011 Mar

PMID : 21344635






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Niemann-Pick disease type C (NPC) is a rare autosomal recessive lysosomal storage disorder characterized by defective intracellular lipid trafficking, with secondary accumulation of free cholesterol, sphingosine, and glycosphingolipids. Sphingosine NPC intracellular cholesterol transporter 1 Homo sapiens
2 Niemann-Pick disease type C (NPC) is a rare autosomal recessive lysosomal storage disorder characterized by defective intracellular lipid trafficking, with secondary accumulation of free cholesterol, sphingosine, and glycosphingolipids. Sphingosine NPC intracellular cholesterol transporter 1 Homo sapiens