Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome-Reference-Cited by-同舟云学术

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Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome

Published:2008-03-12 Issue:16 Volume:70 Page:1313-1321
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Neul J. L.,Fang P.,Barrish J.,Lane J.,Caeg E. B.,Smith E. O.,Zoghbi H.,Percy A.,Glaze D. G.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 402 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Respiratory Disorders in Rett Syndrome;Current Respiratory Medicine Reviews;2025-02

2. Exploring the Clinical Utility of Targeted MECP2 Testing in Real-World Practice;Pediatric Neurology;2024-12

3. Rett Syndrome: The Emerging Landscape of Treatment Strategies;CNS Drugs;2024-09-09

4. Differential dynamics specify MeCP2 function at nucleosomes and methylated DNA;Nature Structural & Molecular Biology;2024-08-20

5. Rett syndrome: The Natural History Study journey;Annals of the Child Neurology Society;2024-08-11

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