Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly-Reference-Cited by-同舟云学术

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Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly

Published:2010-05-18 Issue:3 Volume:3 Page:137-141
ISSN:1939-3792
Container-title:Autism Research
language:en
Short-container-title:Autism Res

Author:

McBride Kim L.,Varga Elizabeth A.,Pastore Matthew T.,Prior Thomas W.,Manickam Kandamurugu,Atkin Joan F.,Herman Gail E.

Publisher

Wiley

Subject

Genetics (clinical),Neurology (clinical),General Neuroscience

Reference25 articles.

1. Advances in autism genetics: On the threshold of a new neurobiology;Abrahams;Nature Reviews Genetics,2008

2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nature Genetics,1999

3. Autism and tuberous sclerosis complex: Prevalence and clinical features;Baker;Journal of Autism and Developmental Disorders,1998

4. Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations;Butler;Journal of Medical Genetics,2005

5. Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly;Buxbaum;American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics,2007

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3. Behavioural, developmental and psychological characteristics in children with germline PTEN mutations: a carer report study;Journal of Intellectual Disability Research;2024-03-20

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