Iossifov I et al. (2014). The contribution of de novo coding mutations to autism spectrum disorder. Nature. 515 [PubMed]

See more from authors: Iossifov I · O'Roak BJ · Sanders SJ · Ronemus M · Krumm N · Levy D · Stessman HA · Witherspoon KT · Vives L · Patterson KE · Smith JD · Paeper B · Nickerson DA · Dea J · Dong S · Gonzalez LE · Mandell JD · Mane SM · Murtha MT · Sullivan CA · Walker MF · Waqar Z · Wei L · Willsey AJ · Yamrom B · Lee YH · Grabowska E · Dalkic E · Wang Z · Marks S · Andrews P · Leotta A · Kendall J · Hakker I · Rosenbaum J · Ma B · Rodgers L · Troge J · Narzisi G · Yoon S · Schatz MC · Ye K · McCombie WR · Shendure J · Eichler EE · State MW · Wigler M

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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