Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations

  1. Toma, C.
  2. Torrico, B.
  3. Hervás, A.
  4. Valdés-Mas, R.
  5. Tristán-Noguero, A.
  6. Padillo, V.
  7. Maristany, M.
  8. Salgado, M.
  9. Arenas, C.
  10. Puente, X.S.
  11. Bayés, M.
  12. Cormand, B.
Journal:
Molecular Psychiatry

ISSN: 1476-5578 1359-4184

Year of publication: 2014

Volume: 19

Issue: 7

Pages: 784-790

Type: Article

DOI: 10.1038/MP.2013.106 GOOGLE SCHOLAR lock_openOpen access editor