Rare and de novo coding variants in chromodomain genes in Chiari I malformation.
Journal Article
Full Text
Duke Authors
Cited Authors
- Sadler, B; Wilborn, J; Antunes, L; Kuensting, T; Hale, AT; Gannon, SR; McCall, K; Cruchaga, C; Harms, M; Voisin, N; Reymond, A; Cappuccio, G; Brunetti-Pierri, N; Tartaglia, M; Niceta, M; Leoni, C; Zampino, G; Ashley-Koch, A; Urbizu, A; Garrett, ME; Soldano, K; Macaya, A; Conrad, D; Strahle, J; Dobbs, MB; Turner, TN; Shannon, CN; Brockmeyer, D; Limbrick, DD; Gurnett, CA; Haller, G
Published Date
- March 4, 2021
Published In
Volume / Issue
- 108 / 3
Start / End Page
- 530 - 531
PubMed ID
- 33667397
Pubmed Central ID
- PMC8008482
Electronic International Standard Serial Number (EISSN)
- 1537-6605
Digital Object Identifier (DOI)
- 10.1016/j.ajhg.2021.01.014
Language
- eng
Conference Location
- United States