[12] Females with such mutations may be completely normal or have clinical features ranging from mild learning disabilities, to Angelman syndrome, to autism and to RS. Females who appear normal or ...

Rett syndrome is a debilitating condition caused by mutations in the MECP2 gene. Traditional gene therapies for such disorders can result in variable and potentially toxic levels of gene ...

Rett Syndrome is a genetic childhood neurological disorder caused by random mutations of the MECP2 gene on the X chromosome. It predominantly affects girls but can rarely also affect boys. Its ...

Rett syndrome is a devastating neurological disorder caused mainly by mutations in the MECP2 gene found on the X chromosome. The disease causes deficits in brain function that lead to behavioural ...

Scientific research increasingly points to genetic factors as key contributors to Autism Spectrum Disorder (ASD) and ...

The Human Domainome 1—the largest library of human protein variants—reveals the cause of certain genetic disorders, paving ...

Research tells us that autism tends to run in families, and a meta-analysis of 7 twin studies claims that 60 to 90% of the ...

Rett syndrome is a debilitating condition caused by mutations in the MECP2 gene. Traditional gene therapies for such disorders can result in variable and potentially toxic levels of gene expression ...