Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC
Journal Article
Overview
publication date
- November 1, 2017
has subject area
- Actin Cytoskeleton - Filamins
- Contractile Proteins - Filamins
- Cytoskeletal Proteins - Filamins
- High-Throughput Nucleotide Sequencing
- Humans
- Macromolecular Substances - Filamins
- Mutation, Missense
- Neoplasm Proteins
- Nerve Tissue Proteins
- Nervous System Diseases - Dyslexia
- Nervous System Diseases - Dyslexia
- Neurodevelopmental Disorders - Dyslexia
- Signs and Symptoms - Dyslexia
- Signs and Symptoms - Dyslexia
has restriction
- hybrid
Date in CU Experts
- September 6, 2017 4:15 AM
Full Author List
- Adams AK; Smith SD; Truong DT; Willcutt EG; Olson RK; DeFries JC; Pennington BF; Gruen JR
author count
- 8
citation count
- 7
published in
- Human Genetics Journal
Other Profiles
International Standard Serial Number (ISSN)
- 0340-6717
Electronic International Standard Serial Number (EISSN)
- 1432-1203
Digital Object Identifier (DOI)
Additional Document Info
start page
- 1395
end page
- 1405
volume
- 136
issue
- 11-12