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Emerging Links Between Pediatric Lysosomal Storage Diseases and Adult Parkinsonism

Lysosomal storage disorders (LSDs) comprise a clinically heterogeneous group of autosomal recessive or X-linked genetic syndromes caused by disruption of lysosomal biogenesis or function resulting in the accumulation of non-degraded substrates. Although LSDs are diagnosed predominantly in children,...

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Bibliografische gegevens
Gepubliceerd in:Mov Disord
Hoofdauteurs: Ysselstein, Daniel, Shulman, Joshua M., Krainc, Dimitri
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2019
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6520126/
https://ncbi.nlm.nih.gov/pubmed/30726573
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.27631
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