Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder

Authors

Reham Khalaf-Nazzal, Arab American University of Palestine
Jennifer L Griffith, Washington University School of Medicine in St. Louis
Joseph R Walsh, Washington University School of Medicine in St. Louis
Amber Neilson, Washington University School of Medicine in St. Louis
Evguenia Kouranova, Washington University School of Medicine in St. Louis
Xiaoxia Cui, Washington University School of Medicine in St. Louis
David T Curiel, Washington University School of Medicine in St. Louis
et al.

Journal

American Journal of Human Genetics

Publication Date

11-3-2022

Volume

109

Issue

11

First Page

2068

Last Page

2079

Document Type

Open Access Publication

DOI

10.1016/j.ajhg.2022.09.012

Rights and Permissions

Khalaf-Nazzal R, Fasham J, Inskeep KA, Blizzard LE, Leslie JS, Wakeling MN, Ubeyratna N, Mitani T, Griffith JL, Baker W, Al-Hijawi F, Keough KC, Gezdirici A, Pena L, Spaeth CG, Turnpenny PD, Walsh JR, Ray R, Neilson A, Kouranova E, Cui X, Curiel DT, Pehlivan D, Akdemir ZC, Posey JE, Lupski JR, Dobyns WB, Stottmann RW, Crosby AH, Baple EL. Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder. Am J Hum Genet. 2022 Nov 3;109(11):2068-2079. doi: 10.1016/j.ajhg.2022.09.012. Copyright 2022 The Authors. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

Recommended Citation

Khalaf-Nazzal, Reham; Griffith, Jennifer L; Walsh, Joseph R; Neilson, Amber; Kouranova, Evguenia; Cui, Xiaoxia; Curiel, David T; and et al., "Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder." American Journal of Human Genetics. 109, 11. 2068 - 2079. (2022).
https://digitalcommons.wustl.edu/oa_4/1584

Department

ICTS (Institute of Clinical and Translational Sciences)

Additional Links

Supplemental material is available for this article at publisher site.