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MBD5 gene

Known as: FLJ11113, methyl-CpG binding domain protein 5, KIAA1461 
National Institutes of Health

Papers overview

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2017
2017
Autism spectrum disorder is a developmental condition of early childhood onset, which impacts socio-communicative functioning and… Expand
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Highly Cited
2014
Highly Cited
2014
Microdeletions of chromosomal region 2q23.1 that disrupt MBD5 (methyl-CpG-binding domain protein 5) contribute to a spectrum of… Expand
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2014
2014
Copy number variations associated with abnormal gene dosage have an important role in the genetic etiology of many… Expand
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2014
2014
2q23.1 microdeletion syndrome is characterized by intellectual disability, motor delay, autistic‐like behaviors, and a… Expand
Highly Cited
2012
Highly Cited
2012
The methyl‐CpG‐binding domain (MBD) gene family was first linked to autism over a decade ago when Rett syndrome, which falls… Expand
2012
2012
We report a 2-year-old female who initially presented with seizures, developmental delay and dysmorphic features and was found to… Expand
Highly Cited
2010
Highly Cited
2010
Microdeletion of chromosome 2q23.1 results in a novel syndrome previously reported in five individuals. Many of the del(2)(q23.1… Expand
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Highly Cited
2010
Highly Cited
2010
Background MBD5 and MBD6 are two uncharacterized mammalian proteins that contain a putative Methyl-Binding Domain (MBD). In the… Expand
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2010
2010
Correction to: European Journal of Human Genetics (2010) 18, 163–170; doi:10.1038/ejhg.2009.152; published online 7 October 2009… Expand
Highly Cited
2002
Highly Cited
2002
BackgroundMethylation at CpG dinucleotides in genomic DNA is a fundamental epigenetic mechanism of gene expression control in… Expand
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