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

  • February 4, 2021

Published In

Volume / Issue

  • 108 / 2

Start / End Page

  • 368 -

PubMed ID

  • 33545031

Pubmed Central ID

  • PMC7895838

Electronic International Standard Serial Number (EISSN)

  • 1537-6605

Digital Object Identifier (DOI)

  • 10.1016/j.ajhg.2020.12.015

Language

  • eng

Conference Location

  • United States