Intellectual disability and autism spectrum disorders: Causal genes and molecular mechanisms-Reference-Cited by-同舟云学术

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Intellectual disability and autism spectrum disorders: Causal genes and molecular mechanisms

Published:2014-10 Issue: Volume:46 Page:161-174
ISSN:0149-7634
Container-title:Neuroscience & Biobehavioral Reviews
language:en
Short-container-title:Neuroscience & Biobehavioral Reviews

Author:

Srivastava Anand K.,Schwartz Charles E.

Funder

National Institute of Child Health and Human Development

National Institute of Neurological Disorders and Stroke

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Cognitive Neuroscience,Neuropsychology and Physiological Psychology

Reference201 articles.

1. Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature;Abou Jamra;Am. J. Hum. Genet.,2011

2. A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders;Addington;Mol. Psychiatry,2011

3. PAK3 mutation in nonsyndromic X-linked mental retardation;Allen;Nat. Genet.,1998

4. Diagnostic Criteria From DSM-IV-TR;American Psychiatric Association,2000

5. Individual common variants exert weak effects on the risk for autism spectrum disorders;Anney;Hum. Mol. Genet.,2012

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