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MECP2 gene

Known as: MECP2, METHYL-CpG-BINDING PROTEIN 2, Methyl CpG Binding Protein 2 (Rett Syndrome) Gene 
This gene plays a role in both the recognition of DNA methylation and the regulation of transcription.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Rett syndrome (RTT) is a neurodevelopmental disorder that results from mutations in the X-linked gene for methyl-CpG-binding… Expand
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2016
2016
Rett syndrome is a severe X-linked dominant neurodevelopmental disorder. Mutations in the MECP2 gene on chromosome Xq28 have been… Expand
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2016
2016
Rett syndrome (RTT) whose major cause is the mutations in the X-linked MECP2 gene is a genetic disease that affects females. We… Expand
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2015
2015
Methyl-CpG binding protein 2 (MeCP2) is a chromatin regulator highly expressed in mature neurons. Mutations of MECP2 gene cause… Expand
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2015
2015
  • J. Millichap
  • Pediatric neurology briefs
  • 2015
  • Corpus ID: 32563163
Investigators from the Boston Children's Hospital recorded pattern-reversal visual evoked potentials (VEPs) in Mecp2 heterozygous… Expand
2013
2013
Rett syndrome (RTT) is a neurodevelopmental disorder characterized by developmental regression beginning 6-18months after birth… Expand
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2010
2010
Streszczenie Zespol Retta (RTT) jest postepującą chorobą zaburzającą rozwoj ukladu nerwowego, ktora jest dziedziczona w sposob… Expand
Highly Cited
2005
Highly Cited
2005
Rett syndrome (RTT; MIM 312750) is a neurodevelopmental disorder with an onset in early childhood that affects 1/10 000–1/15 000… Expand