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

Celestino-Soper PB, Violante S, Crawford EL, Luo R, Lionel AC, Delaby E, Cai G, Sadikovic B, Lee K, Lo C, Gao K, Person RE, Moss TJ, German JR, Huang N, Shinawi M, Treadwell-Deering D, Szatmari P, Roberts W, Fernandez B, Schroer RJ, Stevenson RE, Buxbaum JD, Betancur C, Scherer SW, Sanders SJ, Geschwind DH, Sutcliffe JS, Hurles ME, Wanders RJ, Shaw CA, Leal SM, Cook EH Jr, Goin-Kochel RP, Vaz FM, Beaudet AL

Open source

DOI: 10.1073/pnas.1120210109
Published: 2012 May 22
Container: Proceedings of the National Academy of Sciences of the United States of America
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1073/pnas.1120210109,
  title = {A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.},
  author = {Celestino-Soper PB and Violante S and Crawford EL and Luo R and Lionel AC and Delaby E and Cai G and Sadikovic B and Lee K and Lo C and Gao K and Person RE and Moss TJ and German JR and Huang N and Shinawi M and Treadwell-Deering D and Szatmari P and Roberts W and Fernandez B and Schroer RJ and Stevenson RE and Buxbaum JD and Betancur C and Scherer SW and Sanders SJ and Geschwind DH and Sutcliffe JS and Hurles ME and Wanders RJ and Shaw CA and Leal SM and Cook EH Jr and Goin-Kochel RP and Vaz FM and Beaudet AL},
  year = {2012},
  journal = {Proceedings of the National Academy of Sciences of the United States of America},
  doi = {10.1073/pnas.1120210109},
  url = {https://doi.org/10.1073/pnas.1120210109}
}

RIS

TY  - JOUR
TI  - A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.
AU  - Celestino-Soper PB
AU  - Violante S
AU  - Crawford EL
AU  - Luo R
AU  - Lionel AC
AU  - Delaby E
AU  - Cai G
AU  - Sadikovic B
AU  - Lee K
AU  - Lo C
AU  - Gao K
AU  - Person RE
AU  - Moss TJ
AU  - German JR
AU  - Huang N
AU  - Shinawi M
AU  - Treadwell-Deering D
AU  - Szatmari P
AU  - Roberts W
AU  - Fernandez B
AU  - Schroer RJ
AU  - Stevenson RE
AU  - Buxbaum JD
AU  - Betancur C
AU  - Scherer SW
AU  - Sanders SJ
AU  - Geschwind DH
AU  - Sutcliffe JS
AU  - Hurles ME
AU  - Wanders RJ
AU  - Shaw CA
AU  - Leal SM
AU  - Cook EH Jr
AU  - Goin-Kochel RP
AU  - Vaz FM
AU  - Beaudet AL
PY  - 2012
JO  - Proceedings of the National Academy of Sciences of the United States of America
DO  - 10.1073/pnas.1120210109
UR  - https://doi.org/10.1073/pnas.1120210109
ER  -

APA

PB, C., S, V., EL, C., R, L., AC, L., E, D., G, C., B, S., K, L., C, L., K, G., RE, P., TJ, M., JR, G., N, H., M, S., D, T., P, S., W, R., B, F., RJ, S., RE, S., JD, B., C, B., SW, S., SJ, S., DH, G., JS, S., ME, H., RJ, W., CA, S., SM, L., Jr, C. E., RP, G., FM, V., & AL, B. (2012). A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.. Proceedings of the National Academy of Sciences of the United States of America. https://doi.org/10.1073/pnas.1120210109

Source records

pubmed · retrieved 2026-09-26T13:13:43.952Z