A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability.

Mosca-Boidron AL, Gueneau L, Huguet G, Goldenberg A, Henry C, Gigot N, Pallesi-Pocachard E, Falace A, Duplomb L, Thevenon J, Duffourd Y, St-Onge J, Chambon P, Rivière JB, Thauvin-Robinet C, Callier P, Marle N, Payet M, Ragon C, Goubran Botros H, Buratti J, Calderari S, Dumas G, Delorme R, Lagarde N, Pinoit JM, Rosier A, Masurel-Paulet A, Cardoso C, Mugneret F, Saugier-Veber P, Campion D, Faivre L, Bourgeron T

Open source

DOI: 10.1038/ejhg.2015.211
Published: 2016 Jun
Container: European journal of human genetics : EJHG
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1038/ejhg.2015.211,
  title = {A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability.},
  author = {Mosca-Boidron AL and Gueneau L and Huguet G and Goldenberg A and Henry C and Gigot N and Pallesi-Pocachard E and Falace A and Duplomb L and Thevenon J and Duffourd Y and St-Onge J and Chambon P and Rivière JB and Thauvin-Robinet C and Callier P and Marle N and Payet M and Ragon C and Goubran Botros H and Buratti J and Calderari S and Dumas G and Delorme R and Lagarde N and Pinoit JM and Rosier A and Masurel-Paulet A and Cardoso C and Mugneret F and Saugier-Veber P and Campion D and Faivre L and Bourgeron T},
  year = {2016},
  journal = {European journal of human genetics : EJHG},
  doi = {10.1038/ejhg.2015.211},
  url = {https://doi.org/10.1038/ejhg.2015.211}
}

RIS

TY  - JOUR
TI  - A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability.
AU  - Mosca-Boidron AL
AU  - Gueneau L
AU  - Huguet G
AU  - Goldenberg A
AU  - Henry C
AU  - Gigot N
AU  - Pallesi-Pocachard E
AU  - Falace A
AU  - Duplomb L
AU  - Thevenon J
AU  - Duffourd Y
AU  - St-Onge J
AU  - Chambon P
AU  - Rivière JB
AU  - Thauvin-Robinet C
AU  - Callier P
AU  - Marle N
AU  - Payet M
AU  - Ragon C
AU  - Goubran Botros H
AU  - Buratti J
AU  - Calderari S
AU  - Dumas G
AU  - Delorme R
AU  - Lagarde N
AU  - Pinoit JM
AU  - Rosier A
AU  - Masurel-Paulet A
AU  - Cardoso C
AU  - Mugneret F
AU  - Saugier-Veber P
AU  - Campion D
AU  - Faivre L
AU  - Bourgeron T
PY  - 2016
JO  - European journal of human genetics : EJHG
DO  - 10.1038/ejhg.2015.211
UR  - https://doi.org/10.1038/ejhg.2015.211
ER  -

APA

AL, M., L, G., G, H., A, G., C, H., N, G., E, P., A, F., L, D., J, T., Y, D., J, S., P, C., JB, R., C, T., P, C., N, M., M, P., C, R., H, G. B., J, B., S, C., G, D., R, D., N, L., JM, P., A, R., A, M., C, C., F, M., P, S., D, C., L, F., & T, B. (2016). A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability.. European journal of human genetics : EJHG. https://doi.org/10.1038/ejhg.2015.211

Source records

pubmed · retrieved 2026-09-27T12:21:29.446Z
europe-pmc · retrieved 2026-09-27T12:21:29.460Z
hal · retrieved 2026-09-27T12:21:29.485Z