Refining the Phenotype of Common Mutations in Rett Syndrome

Journal of Medical Genetics - United Kingdom
doi 10.1136/jmg.2003.011130
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

BMJ

Related search

MeCP2 Mutations in Children With and Without the Phenotype of Rett Syndrome

Neurology
Neurology
2001English

Genotype-Phenotype Correlation in Brazillian Rett Syndrome Patients

Arquivos de Neuro-Psiquiatria
Biological PsychiatryNeurology
2009English

MECP2 Mutations Associated With Rett Syndrome - Molecular Approaches

Journal of Neonatal Biology
2016English

Rett Syndrome.

Journal of Medical Genetics
Genetics
1996English

Atypical Rett Syndrome

2020English

Specific Mutations in Methyl-CpG-Binding Protein 2 Confer Different Severity in Rett Syndrome

Neurology
Neurology
2008English

Rett Syndrome and MeCP2

NeuroMolecular Medicine
Molecular NeuroscienceNeurologyMolecular MedicineCellular
2014English

The American History of Rett Syndrome

Pediatric Neurology
Child HealthDevelopmental NeurosciencePediatricsPerinatologyNeurology
2014English

Microvascular Abnormalities in Rett Syndrome

Clinical Hemorheology and Microcirculation
PhysiologyCardiovascular MedicineHematologyCardiology
2013English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy