A rapid whole-genome sequencing service for infants with rare diseases in the United Arab Emirates

Nat Med. 2023 Dec;29(12):2979-2980. doi: 10.1038/s41591-023-02596-x.
No abstract available

Publication types

  • Letter

MeSH terms

  • Humans
  • Rare Diseases* / epidemiology
  • Rare Diseases* / genetics
  • Rare Diseases* / therapy
  • United Arab Emirates / epidemiology
  • Whole Genome Sequencing