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A familial heterozygous null mutation of MET in autism spectrum disorder

(2014) AUTISM RESEARCH. 7(5). p.617-622
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c-MET, autism spectrum disorder, social brain, neurodevelopment, RECEPTOR TYROSINE KINASE, DE-NOVO MUTATIONS, BRAIN-DEVELOPMENT, MOUSE FOREBRAIN, GENETIC VARIANT, ASSOCIATION, EXPRESSION, RISK

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Citation

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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.
@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},
}

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