Lek M et al. (2016). Analysis of protein-coding genetic variation in 60,706 humans. Nature. 536 [PubMed]

See more from authors: Lek M · Karczewski KJ · Minikel EV · Samocha KE · Banks E · Fennell T · O'Donnell-Luria AH · Ware JS · Hill AJ · Cummings BB · Tukiainen T · Birnbaum DP · Kosmicki JA · Duncan LE · Estrada K · Zhao F · Zou J · Pierce-Hoffman E · Berghout J · Cooper DN · Deflaux N · DePristo M · Do R · Flannick J · Fromer M · Gauthier L · Goldstein J · Gupta N · Howrigan D · Kiezun A · Kurki MI · Moonshine AL · Natarajan P · Orozco L · Peloso GM · Poplin R · Rivas MA · Ruano-Rubio V · Rose SA · Ruderfer DM · Shakir K · Stenson PD · Stevens C · Thomas BP · Tiao G · Tusie-Luna MT · Weisburd B · Won HH · Yu D · Altshuler DM · Ardissino D · Boehnke M · Danesh J · Donnelly S · Elosua R · Florez JC · Gabriel SB · Getz G · Glatt SJ · Hultman CM · Kathiresan S · Laakso M · McCarroll S · McCarthy MI · McGovern D · McPherson R · Neale BM · Palotie A · Purcell SM · Saleheen D · Scharf JM · Sklar P · Sullivan PF · Tuomilehto J · Tsuang MT · Watkins HC · Wilson JG · Daly MJ · MacArthur DG · Exome Aggregation Consortium

References and models cited by this paper
References and models that cite this paper

Ben-Shalom R et al. (2017). Opposing Effects on NaV1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile Seizures. Biological psychiatry. 82 [PubMed]

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