Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC.
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| Title: | Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC. |
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| Authors: | Adams AK; Department of Genetics, Yale University, New Haven, CT, USA., Smith SD; Munroe Meyer Institute, University of Nebraska Medical Center, Omaha, NE, USA., Truong DT; Department of Pediatrics, Yale University, New Haven, CT, USA., Willcutt EG; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA.; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA., Olson RK; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA.; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA., DeFries JC; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA.; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA., Pennington BF; Department of Psychology, University of Denver, Denver, CO, USA., Gruen JR; Department of Genetics, Yale University, New Haven, CT, USA. jeffrey.gruen@yale.edu.; Department of Pediatrics and the Investigative Medicine Program, Yale University, New Haven, CT, USA. jeffrey.gruen@yale.edu. |
| Source: | Human genetics [Hum Genet] 2017 Nov; Vol. 136 (11-12), pp. 1395-1405. Date of Electronic Publication: 2017 Sep 02. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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