As MeCP2 acts a multifunctional regulator of gene transcription, knowing the gene mutation is sufficient to make a diagnosis, but this information is not sufficient to understand the mechanisms by which, the MECP2 gene mutation drives the clinical manifestations in this complex neurodevelopmental disease
Rett syndrome (RTT) is an orphan progressive neurodevelopmental disease affecting almost exclusively...
Rett syndrome (RTT) is a severe neurological disorder caused by mutations in the gene encoding methy...
Rett syndrome (RTT) is a rare disease but still one of the most abundant causes for intellectual dis...
As MeCP2 acts a multifunctional regulator of gene transcription, knowing the gene mutation is suffic...
International audienceThe main cause of Rett syndrome (RTT), a pervasive development disorder almost...
The main cause of Rett syndrome (RTT), a pervasive development disorder almost exclusively affecting...
Rett syndrome (RTT, MIM 312750) is a rare and orphan progressive neurodevelopmental disorder affecti...
Modulation of oxidative stress response in neurodevelopment disorders. The case of the Rett syndrome...
The oxidative stress (OS) hypothesis is able to explain several features of Rett syndrome (RTT), a p...
Rett syndrome (RTT) is a rare neurodevelopmental disorder affecting almost exclusively females, caus...
Rett syndrome (RTT) and MECP2 duplication syndrome (MDS) are neurodevelopmental disorders caused by ...
Rett syndrome (RTT) is a devastating genetic disorder that worldwide represents the most common gene...
Genetic mutations of the X-linked gene MECP2, encoding methyl-CpG-binding protein 2, cause Rett synd...
AbstractRett syndrome (RTT) is a rare neurodevelopmental disorder affecting almost exclusively femal...
Rett syndrome (RTT) is an orphan progressive neurodevelopmental disease affecting almost exclusively...
Rett syndrome (RTT) is a severe neurological disorder caused by mutations in the gene encoding methy...
Rett syndrome (RTT) is a rare disease but still one of the most abundant causes for intellectual dis...
As MeCP2 acts a multifunctional regulator of gene transcription, knowing the gene mutation is suffic...
International audienceThe main cause of Rett syndrome (RTT), a pervasive development disorder almost...
The main cause of Rett syndrome (RTT), a pervasive development disorder almost exclusively affecting...
Rett syndrome (RTT, MIM 312750) is a rare and orphan progressive neurodevelopmental disorder affecti...
Modulation of oxidative stress response in neurodevelopment disorders. The case of the Rett syndrome...
The oxidative stress (OS) hypothesis is able to explain several features of Rett syndrome (RTT), a p...
Rett syndrome (RTT) is a rare neurodevelopmental disorder affecting almost exclusively females, caus...
Rett syndrome (RTT) and MECP2 duplication syndrome (MDS) are neurodevelopmental disorders caused by ...
Rett syndrome (RTT) is a devastating genetic disorder that worldwide represents the most common gene...
Genetic mutations of the X-linked gene MECP2, encoding methyl-CpG-binding protein 2, cause Rett synd...
AbstractRett syndrome (RTT) is a rare neurodevelopmental disorder affecting almost exclusively femal...
Rett syndrome (RTT) is an orphan progressive neurodevelopmental disease affecting almost exclusively...
Rett syndrome (RTT) is a severe neurological disorder caused by mutations in the gene encoding methy...
Rett syndrome (RTT) is a rare disease but still one of the most abundant causes for intellectual dis...
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