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The implications of de novo coding mutations in simplex autism families
Author(s) -
Utami K. H.
Publication year - 2015
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.12582
Subject(s) - coding (social sciences) , citation , computer science , agency (philosophy) , psychology , library science , sociology , epistemology , philosophy , social science
1. O’Roak BJ, Vives L, Girirajan S et al. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature 2012: 485: 246–250. 2. Iossifov I, Ronemus M, Levy D et al. De novo gene disruptions in children on the autistic spectrum. Neuron 2012: 74: 285–299. 3. Iossifov I, O’Roak BJ, Sanders SJ et al. The contribution of de novo coding mutations to autism spectrum disorder. Nature 2014: 525 (7526): 216–221. 4. Michaelson JJ, Shi Y, Gujral M et al. Whole-genome sequencing in autism identifies hot spots for de novo germline mutation. Cell 2012: 151: 1431–1442.