Sanders SJ et al. (2012). De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature. 485 [PubMed]

See more from authors: Sanders SJ · Murtha MT · Gupta AR · Murdoch JD · Raubeson MJ · Willsey AJ · Ercan-Sencicek AG · DiLullo NM · Parikshak NN · Stein JL · Walker MF · Ober GT · Teran NA · Song Y · El-Fishawy P · Murtha RC · Choi M · Overton JD · Bjornson RD · Carriero NJ · Meyer KA · Bilguvar K · Mane SM · Sestan N · Lifton RP · Günel M · Roeder K · Geschwind DH · Devlin B · State MW

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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