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Cathepsin D Polymorphism C224T in Childhood-Onset Neurodegenerative Disorders: No Impact for Childhood Dementia
Compromised lysosomal functioning has been identified as a major risk factor for neurodegenerative disorders such as Alzheimer's and Parkinson's diseases. Furthermore, the association between a defined cathepsin D ( CTSD ) polymorphism and a higher risk of sporadic Alzheimer's disease...
Tallennettuna:
| Julkaisussa: | J Pediatr Genet |
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| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Georg Thieme Verlag KG
2018
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| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5809166/ https://ncbi.nlm.nih.gov/pubmed/29441216 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0037-1607341 |
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