z-logo
Premium
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.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom