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Molecular characterization of PRKN structural variations identified through whole‐genome sequencing
BACKGROUND: Early‐onset Parkinson's disease (PD) is the most common inherited form of parkinsonism, with the PRKN gene being the most frequently identified mutated. Exon rearrangements, identified in about 43.2% of the reported PD patients and with higher frequency in specific ethnicities, are...
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| Gepubliceerd in: | Mol Genet Genomic Med |
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| Hoofdauteurs: | , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
John Wiley and Sons Inc.
2018
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6305656/ https://ncbi.nlm.nih.gov/pubmed/30328284 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.482 |
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