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Rett syndrome
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
MECP2
SPATA22
FOXG1
MRXSL
LINC01139
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
GTAAACC_MIR2995P
Methyl-CpG binding protein MeCP2
positive regulation of DNA methylation
positive regulation of histone H3-K9 trimethylation
negative regulation of transcription from RNA polymerase II promoter involved in smooth muscle cell differentiation
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Curated Studies
Most Correlated Studies
Brains from 6wk old MECP2 knockout mice (Rett syndrome model) injected 2wk daily with valproic acid
Mouse Phenotypes - Autistic continuum
OMIM - Mental retardation
Superior frontal gyrus of girls with Rett syndrome
OMIM - Intellectual disability
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Literature
Most Relevant Literature
Rett syndrome and menstruation.
Treating hypoxia in a feeble breather with Rett syndrome.
Revealing the complexity of a monogenic disease: rett syndrome exome sequencing.
Genetic and epileptic features in Rett syndrome.
Rett syndrome: an eye-tracking study of attention and recognition memory.
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Clinical Trials
Most Relevant Clinical Trials
The Findings of MR Imaging in Rett Syndrome
Patients With RETT Syndrome
Biobanking of Rett Syndrome and Related Disorders
Functional Abilities in Rett Syndrome
Osteoporosis in RETT Syndrome
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