Heterozygous FA2H mutations in autism spectrum disorders

Isabelle Scheid, Anna Maruani, Guillaume Huguet, Claire S Leblond, Gudrun Nygren, Henrik Anckarsäter, Anita Beggiato, Maria Rastam, Fréderique Amsellem, I Carina Gillberg, Monique Elmaleh, Marion Leboyer, Christopher Gillberg, Catalina Betancur, Mary Coleman, Hiroko Hama, Edwin H Cook, Thomas Bourgeron, Richard Delorme

Open source

DOI
10.1186/1471-2350-14-124
Published
2013-12
Container
BMC Medical Genetics
Publisher
Springer Science and Business Media LLC
Open access
unknown

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BibTeX

@article{allodium:10.1186/1471-2350-14-124,
  title = {Heterozygous FA2H mutations in autism spectrum disorders},
  author = {Isabelle Scheid and Anna Maruani and Guillaume Huguet and Claire S Leblond and Gudrun Nygren and Henrik Anckarsäter and Anita Beggiato and Maria Rastam and Fréderique Amsellem and I Carina Gillberg and Monique Elmaleh and Marion Leboyer and Christopher Gillberg and Catalina Betancur and Mary Coleman and Hiroko Hama and Edwin H Cook and Thomas Bourgeron and Richard Delorme},
  year = {2013},
  journal = {BMC Medical Genetics},
  doi = {10.1186/1471-2350-14-124},
  url = {https://doi.org/10.1186/1471-2350-14-124}
}

RIS

TY  - JOUR
TI  - Heterozygous FA2H mutations in autism spectrum disorders
AU  - Isabelle Scheid
AU  - Anna Maruani
AU  - Guillaume Huguet
AU  - Claire S Leblond
AU  - Gudrun Nygren
AU  - Henrik Anckarsäter
AU  - Anita Beggiato
AU  - Maria Rastam
AU  - Fréderique Amsellem
AU  - I Carina Gillberg
AU  - Monique Elmaleh
AU  - Marion Leboyer
AU  - Christopher Gillberg
AU  - Catalina Betancur
AU  - Mary Coleman
AU  - Hiroko Hama
AU  - Edwin H Cook
AU  - Thomas Bourgeron
AU  - Richard Delorme
PY  - 2013
JO  - BMC Medical Genetics
DO  - 10.1186/1471-2350-14-124
UR  - https://doi.org/10.1186/1471-2350-14-124
ER  - 

APA

Scheid, I., Maruani, A., Huguet, G., Leblond, C. S., Nygren, G., Anckarsäter, H., Beggiato, A., Rastam, M., Amsellem, F., Gillberg, I. C., Elmaleh, M., Leboyer, M., Gillberg, C., Betancur, C., Coleman, M., Hama, H., Cook, E. H., Bourgeron, T., & Delorme, R. (2013). Heterozygous FA2H mutations in autism spectrum disorders. BMC Medical Genetics. https://doi.org/10.1186/1471-2350-14-124

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