Niemann-Pick disease type C

Niemann-Pick disease type C is an autosomal recessive neurodegenerative lysosomal storage disorder characterized by impaired cellular trafficking of cholesterol and sphingolipids and caused by mutations in either the NPC1 or NPC2 gene. The age of presentation is highly variable, ranging from the…

Recent advances in the treatment of Niemann pick disease type C: A

Niemann-Pick-C desease - CERMO-FC

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Health Tip on New Treatment that Shows Promise in Niemann-Pick

Therapeutic intervention for Niemann–Pick type C disease must

Progression of Niemann–Pick type C disease in mice and humans

Niemann–Pick disease type C1 (NPC1) is associated with early-onset

What is Niemann Pick Type C - Race for Adam

Niemann-Pick disease type C Orphanet Journal of Rare Diseases

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Morphology of Niemann-Pick type C metabolic storage disorder

Niemann–Pick Disease Type C

Patient with Niemann-Pick disease type C: over 20 years' follow-up