Open AccessEvaluation of seizures and clinical features of pediatric patients diagnosed with Rett Syndrome who were detected to have MECP2 mutation
Author(s) -
Serkan Kırık,
Mahmut Aslan,
Bilge Özgör,
Serdal Güngör
Publication year - 2021
Publication title -
turkish journal of clinics and laboratory
Language(s) - English
Resource type - Journals
ISSN - 2149-8296
DOI - 10.18663/tjcl.578475
Subject(s) - rett syndrome , mecp2 , medicine , pediatrics , neurodevelopmental disorder , psychomotor learning , clinical diagnosis , disease , psychiatry , autism , pathology , genetics , cognition , gene , biology , phenotype
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