Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry.
BACKGROUND: Autism spectrum disorders (ASDs) are a group of highly heritable neurodevelopmental disorders which are characteristically comprised of impairments in social interaction, communication and restricted interests/behaviours. Several cell adhesion transmembrane leucine-rich repeat (LRR) prot...
Κύριοι συγγραφείς: | Sousa, I, Clark, T, Holt, R, Pagnamenta, A, Mulder, E, Minderaa, R, Bailey, A, Battaglia, A, Klauck, S, Poustka, F, Monaco, A |
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Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
2010
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Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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A 15q13.3 microdeletion segregating with autism.
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International molecular genetic study of autism consortium (IMGSAC). Towards identification of autism susceptibility variants in the IMGSAC sample
ανά: Lamb, J, κ.ά.
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Linkage and candidate gene studies of autism spectrum disorders in European populations.
ανά: Holt, R, κ.ά.
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MET and autism susceptibility: family and case-control studies.
ανά: Sousa, I, κ.ά.
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CLERC and centrosomal leucine-rich repeat proteins
ανά: Muto Yoshinori, κ.ά.
Έκδοση: (2010-02-01)