MECP2 Mutation: myoclonic epilepsy and Rett syndrome features in a rare missense variant
Year: 2024
Type: conference-paper
Study design: Case Report
Authors: Layegh Mahsa, Kinton Lucy, Slaght Sean J
Institution: University Hospital Southampton NHS Foundation Trust
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W4404183375