Rare variants and disease

Brief Funct Genomics. 2014 Sep;13(5):351-2. doi: 10.1093/bfgp/elu030.
No abstract available

Publication types

  • Editorial

MeSH terms

  • Genetic Variation / genetics
  • Genome, Human / genetics
  • Genome-Wide Association Study / methods*
  • Genotype
  • High-Throughput Nucleotide Sequencing
  • Humans