Niemann-Pick type C disease is associated with mtDNA disorganization.

Mitochondrial dysfunction in fibroblasts derived from patients with Niemann-Pick type C disease - ScienceDirect

Finding pathogenic commonalities between Niemann-Pick type C and other lysosomal storage disorders: Opportunities for shared therapeutic interventions - ScienceDirect

Niemann-Pick disease type C as a neurovisceral disease. Schematic

Frontiers Inborn Errors of Metabolism Associated With Autism Spectrum Disorders: Approaches to Intervention

Full article: Mechanisms of mitochondrial diseases

Unbiased yeast screens identify cellular pathways affected in Niemann–Pick disease type C

Diagnosing Niemann Pick disease, Type C - ppt download

Niemann-Pick type C disease is associated with mtDNA disorganization.

Niemann-Pick Disease, Type C2

Frontiers “Mitochondrial Toolbox” – A Review of Online Resources to Explore Mitochondrial Genomics

Epidemiological, clinical and biochemical characterization of the p.(Ala359Asp) SMPD1 variant causing Niemann–Pick disease type B

Niemann-Pick Disease, Types A and B

Perspectives in Pediatric Pathology, Chapter 21. Testicular Pathology in Heritable Metabolic Disease - Manuel Nistal, Ricardo Paniagua, Pilar González-Peramato, Miguel Reyes-Múgica, 2016

Molecular basis of Leigh syndrome: a current look, Orphanet Journal of Rare Diseases

Mitochondrial Dysfunction and Neurodegeneration in Lysosomal Storage Disorders: Trends in Molecular Medicine