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Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing.

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Title: Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing.
Authors: Rodin RE; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA.; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA, USA., Dou Y; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA., Kwon M; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA., Sherman MA; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.; Department of Electrical Engineering and Computer Science, MIT, Cambridge, MA, USA.; Division of Genetics, Brigham and Women's Hospital, Boston, MA, USA.; Broad Institute of MIT and Harvard, Cambridge, MA, USA., D'Gama AM; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA.; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA, USA., Doan RN; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA., Rento LM; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA.; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA, USA., Girskis KM; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA.; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA, USA., Bohrson CL; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA., Kim SN; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA.; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA, USA., Nadig A; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA.; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA, USA., Luquette LJ; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA., Gulhan DC; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA., Park PJ; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA. peter_park@hms.harvard.edu.; Division of Genetics, Brigham and Women's Hospital, Boston, MA, USA. peter_park@hms.harvard.edu., Walsh CA; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA. Christopher.walsh@childrens.harvard.edu.; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA, USA. Christopher.walsh@childrens.harvard.edu.; Broad Institute of MIT and Harvard, Cambridge, MA, USA. Christopher.walsh@childrens.harvard.edu.
Corporate Authors: Brain Somatic Mosaicism Network
Source: Nature neuroscience [Nat Neurosci] 2023 Oct; Vol. 26 (10), pp. 1833.
Publication Type: Published Erratum
Journal Info: Publisher: Nature Publishing Group Country of Publication: United States NLM ID: 9809671 Publication Model: Print Cited Medium: Internet ISSN: 1546-1726 (Electronic) Linking ISSN: 10976256 NLM ISO Abbreviation: Nat Neurosci Subsets: MEDLINE; PubMed not MEDLINE
Database: MEDLINE Ultimate
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