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The Discovery of LRRK2 p.Arg1441Ser, a novel mutation for Parkinson’s disease, Adds to the Complexity of a Mutational Hotspot
Mutations in the LRRK2 gene result in autosomal dominant, late onset Parkinson’s disease (PD). Three such mutations (p.Arg1441Cys, p.Arg1441Gly, and p.Arg1441His) are known to occur within codon 1441, and haplotype analyses indicate that each one has arisen independently on multiple occasions. We se...
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| Gepubliceerd in: | Am J Med Genet B Neuropsychiatr Genet |
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| Hoofdauteurs: | , , , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2016
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5028305/ https://ncbi.nlm.nih.gov/pubmed/27111571 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.32452 |
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