Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Reference83 articles.
1. Finding the missing heritability of complex diseases
2. Genomewide Association Studies and Human Disease
3. Towards a complete resolution of the genetic architecture of disease
4. A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease
5. VPS35 Mutations in Parkinson Disease
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