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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

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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
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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2015
2015
Investigators from the Boston Children's Hospital recorded pattern-reversal visual evoked potentials (VEPs) in Mecp2 heterozygous… Expand
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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
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2005
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
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