Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism uri icon

autores

  • Patrícia Espinheira de Sá Maciel
  • Fu, J.M.
  • Satterstrom, F.K.
  • Peng, M.
  • Brand, H.
  • Collins, R.L.
  • Dong, S.
  • Klei, L.
  • et al

data de publicação

  • janeiro 1, 2021