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Niemann-Pick C Disease Gene Mutations and Age-Related Neurodegenerative Disorders
Niemann-Pick type C (NPC) disease is a rare autosomal-recessively inherited lysosomal storage disorder caused by mutations in NPC1 (95%) or NPC2. Given the highly variable phenotype, diagnosis is challenging and particularly late-onset forms with predominantly neuropsychiatric presentations are like...
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3875432/ https://ncbi.nlm.nih.gov/pubmed/24386122 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0082879 |
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