Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability

S. Riazuddin, M. Hussain, A. Razzaq, Z. Iqbal, M. Shahzad, D. L. Polla, Y. Song, E. van Beusekom, A. A. Khan, L. Tomas-Roca, M. Rashid, M. Y. Zahoor, W. M. Wissink-Lindhout, M. A. R. Basra, M. Ansar, Z. Agha, K. van Heeswijk, F. Rasheed, M. Van de Vorst, J. A. VeltmanC. Gilissen, J. Akram, T. Kleefstra, M. Z. Assir, D. Grozeva, K. Carss, F. L. Raymond, T. D. O'Connor, S. A. Riazuddin, S. N. Khan, Z. M. Ahmed, A. P. M. de Brouwer, H. van Bokhoven*, S. Riazuddin*, UK10K

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)1604-1614
Number of pages11
JournalMolecular Psychiatry
Volume22
Issue number11
DOIs
Publication statusPublished - Nov 2017

Keywords

  • NONSYNDROMIC MENTAL-RETARDATION
  • DE-NOVO MUTATIONS
  • COGNITIVE DISORDERS
  • METABOLIC CRISES
  • NETWORKS
  • DEAFNESS
  • AUTISM
  • SCHIZOPHRENIA
  • MORTALITY
  • MARRIAGE

Cite this