Mutations in the calcium-related gene IL1RAPL1 are associated with autism-Reference-Cited by-同舟云学术

Mutations in the calcium-related gene IL1RAPL1 are associated with autism

Published:2008-09-04 Issue:24 Volume:17 Page:3965-3974
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Piton A.,Michaud J. L.,Peng H.,Aradhya S.,Gauthier J.,Mottron L.,Champagne N.,Lafreniere R. G.,Hamdan F. F.,Joober R.,Fombonne E.,Marineau C.,Cossette P.,Dube M.-P.,Haghighi P.,Drapeau P.,Barker P. A.,Carbonetto S.,Rouleau G. A.,

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/17/24/3965/1486684/ddn300.pdf

Reference29 articles.

1. The genetics of autism

2. Autism as a strongly genetic disorder: evidence from a British twin study

3. A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence

4. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

5. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

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