Wagner, Matias
Skorobogatko, Yuliya
Pode-Shakked, Ben
Powell, Cynthia M.
Alhaddad, Bader
Seibt, Annette
Barel, Ortal
Heimer, Gali
Hoffmann, Chen
Demmer, Laurie A.
Perilla-Young, Yezmin
Remke, Marc
Wieczorek, Dagmar
Navaratnarajah, Tharsini
Lichtner, Peter
Klee, Dirk
Shamseldin, Hanan E.
Al Mutairi, Fuad
Mayatepek, Ertan
Strom, Tim
Meitinger, Thomas
Alkuraya, Fowzan S.
Anikster, Yair
Saltiel, Alan R.
Distelmaier, Felix
Funding for this research was provided by:
Deutsche Forschungsgemeinschaft
This article is maintained by: Elsevier
Article Title: Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities
Journal Title: The American Journal of Human Genetics
CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.ajhg.2020.01.002
Content Type: article
Copyright: © 2020 American Society of Human Genetics.