Ghent University Academic Bibliography

Advanced

A familial heterozygous null mutation of MET in autism spectrum disorder

Nelle Lambert, Vanessa Wermenbol, Bruno Pichon, Sandra Acosta, Jelle van den Ameele UGent, Camille Perazzolo, Diana Messina, Maria-Franca Musumeci, Barbara Dessars, Anne De Leener, et al. (2014) AUTISM RESEARCH. 7(5). p.617-622
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
c-MET, autism spectrum disorder, social brain, neurodevelopment, RECEPTOR TYROSINE KINASE, DE-NOVO MUTATIONS, BRAIN-DEVELOPMENT, MOUSE FOREBRAIN, GENETIC VARIANT, ASSOCIATION, EXPRESSION, RISK
journal title
AUTISM RESEARCH
Autism Res.
volume
7
issue
5
pages
617 - 622
Web of Science type
Article
Web of Science id
000343971300010
JCR category
PSYCHOLOGY, DEVELOPMENTAL
JCR impact factor
4.33 (2014)
JCR rank
3/68 (2014)
JCR quartile
1 (2014)
ISSN
1939-3792
DOI
10.1002/aur.1396
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
5668171
handle
http://hdl.handle.net/1854/LU-5668171
date created
2014-08-05 20:59:26
date last changed
2016-12-19 15:39:16
@article{5668171,
  author       = {Lambert, Nelle and Wermenbol, Vanessa and Pichon, Bruno and Acosta, Sandra and van den Ameele, Jelle and Perazzolo, Camille and Messina, Diana and Musumeci, Maria-Franca and Dessars, Barbara and De Leener, Anne and Abramowicz, Marc and Vilain, Catheline},
  issn         = {1939-3792},
  journal      = {AUTISM RESEARCH},
  keyword      = {c-MET,autism spectrum disorder,social brain,neurodevelopment,RECEPTOR TYROSINE KINASE,DE-NOVO MUTATIONS,BRAIN-DEVELOPMENT,MOUSE FOREBRAIN,GENETIC VARIANT,ASSOCIATION,EXPRESSION,RISK},
  language     = {eng},
  number       = {5},
  pages        = {617--622},
  title        = {A familial heterozygous null mutation of MET in autism spectrum disorder},
  url          = {http://dx.doi.org/10.1002/aur.1396},
  volume       = {7},
  year         = {2014},
}

Chicago
Lambert, Nelle, Vanessa Wermenbol, Bruno Pichon, Sandra Acosta, Jelle van den Ameele, Camille Perazzolo, Diana Messina, et al. 2014. “A Familial Heterozygous Null Mutation of MET in Autism Spectrum Disorder.” Autism Research 7 (5): 617–622.
APA
Lambert, N., Wermenbol, V., Pichon, B., Acosta, S., van den Ameele, J., Perazzolo, C., Messina, D., et al. (2014). A familial heterozygous null mutation of MET in autism spectrum disorder. AUTISM RESEARCH, 7(5), 617–622.
Vancouver
1.
Lambert N, Wermenbol V, Pichon B, Acosta S, van den Ameele J, Perazzolo C, et al. A familial heterozygous null mutation of MET in autism spectrum disorder. AUTISM RESEARCH. 2014;7(5):617–22.
MLA
Lambert, Nelle, Vanessa Wermenbol, Bruno Pichon, et al. “A Familial Heterozygous Null Mutation of MET in Autism Spectrum Disorder.” AUTISM RESEARCH 7.5 (2014): 617–622. Print.