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A comprehensive analysis of copy number variation in a Turkish dementia cohort
BACKGROUND: Copy number variants (CNVs) include deletions or multiplications spanning genomic regions. These regions vary in size and may span genes known to play a role in human diseases. As examples, duplications and triplications of SNCA have been shown to cause forms of Parkinson’s disease, whil...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Hum Genomics |
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| Prif Awduron: | , , , , , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BioMed Central
2021
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8317312/ https://ncbi.nlm.nih.gov/pubmed/34321086 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40246-021-00346-z |
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