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Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndromeDOI 10.1093/hmg/ddu496
Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome.Semantic proximity
MeCP2 isoform e1 mutant mice recapitulate motor and metabolic phenotypes of Rett syndromeSemantic proximity
Epigenetic Dysregulation in Rett Syndrome: Multisystem Pathophysiology, MECP2 Isoform-Specific Mechanisms, and Targeted Therapeutic StrategiesSemantic proximity
Epigenetic Dysregulation in Rett Syndrome: Multisystem Pathophysiology, MECP2 Isoform-Specific Mechanisms, and Targeted Therapeutic StrategiesSemantic proximity
MeCP2 isoform e1 mutant mice recapitulate motor and metabolic phenotypes of Rett syndrome.Semantic proximity
The story of Rett syndrome: from clinic to neurobiology.Semantic proximity
Rett Syndrome: A Timely Review From Recognition to Current Clinical Approaches and Clinical Study Updates.Semantic proximity
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome.Semantic proximity
Rett syndrome from bench to bedside: recent advancesSemantic proximity
Mouse models of Rett syndrome: from behavioural phenotyping to preclinical evaluation of new therapeutic approaches.Semantic proximity
Transgenic complementation of MeCP2 deficiency: phenotypic rescue of Mecp2-null mice by isoform-specific transgenes.Semantic proximity
Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome.Semantic proximity
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