A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.

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Source ISSN: 0027-8424
Author Celestino-Soper, Patrícia, B. S., Violante, Sara, Crawford, Emily, L., Luo, Rui, Lionel, Anath, C., Delaby, Elsa, Cai, Guiqing, Sadikovic, Bekim, Lee, Kwanghyuk, Lo, Charlene, Gao, Kun, Person, Richard, E., Moss, Timothy, J., German, Jennifer, R., Huang, Ni, Shinawi, Marwan, Treadwell-Deering, Diane, Szatmari, Peter, Roberts, Wendy, Fernandez, Bridget, Schroer, Richard, J., Stevenson, Roger, E., Buxbaum, Joseph, D., Betancur, Catalina, Scherer, Stephen, W., Sanders, Stephan, J., Geschwind, Daniel, H., Sutcliffe, James, S., Hurles, Matthew, E., Wanders, Ronald, J. A., Shaw, Chad, A., Leal, Suzanne, M., Cook, Edwin, H., Goin-Kochel, Robin, P., Vaz, Frédéric, M., Beaudet, Arthur, L.
Maintainer CCSD
Last Updated May 19, 2026, 10:41 (UTC)
Created May 19, 2026, 10:41 (UTC)
Identifier inserm-00696112
Language en
Rights https://about.hal.science/hal-authorisation-v1/
contributor Department of Molecular and Human Genetics ; Baylor College of Medicine (BCM) ; Baylor University-Baylor University
creator Celestino-Soper, Patrícia, B. S.
date 2012-05-22T00:00:00
harvest_object_id 9c94dc6d-2f79-413a-aaa9-c623291a009e
harvest_source_id 3374d638-d20b-4672-ba96-a23232d55657
harvest_source_title test moissonnage SELUNE
metadata_modified 2026-02-07T00:00:00
relation info:eu-repo/semantics/altIdentifier/doi/10.1073/pnas.1120210109
set_spec type:ART