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Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controls
A novel heterozygous non-synonymous mutation and a novel polymorphism in OMI/HTRA2 locus have been associated with Parkinson's disease (PD) in a German population. In an attempt to replicate these results in an independent population, we analyzed the entire coding region of OMI/HTRA2 in a serie...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2008
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2574854/ https://ncbi.nlm.nih.gov/pubmed/18364387 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn096 |
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