লোডিং...
Identifying rare and common disease associated variants in genomic data using Parkinson’s disease as a model
BACKGROUND: Genome-wide association studies have been successful in identifying common genetic variants for human diseases. However, much of the heritable variation associated with diseases such as Parkinson’s disease remains unknown suggesting that many more risk loci are yet to be identified. Rare...
সংরক্ষণ করুন:
| প্রকাশিত: | J Biomed Sci |
|---|---|
| প্রধান লেখক: | , , , , , , |
| বিন্যাস: | Artigo |
| ভাষা: | Inglês |
| প্রকাশিত: |
BioMed Central
2014
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| বিষয়গুলি: | |
| অনলাইন ব্যবহার করুন: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4428531/ https://ncbi.nlm.nih.gov/pubmed/25175702 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12929-014-0088-9 |
| ট্যাগগুলো: |
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