# <i>Methyl-CpG-binding protein 2</i> (<i>MECP2</i>) mutation type is associated with disease severity in Rett syndrome

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/i-methyl-cpg-binding-protein-2-i-i-mecp2-i-mutation-type-is-associated-with/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Vishnu Anand Cuddapah,Rajesh B Pillai,Kiran V Shekar,Jane B. Lane,Kathleen J. Motil,Steven A. Skinner,Daniel Tarquinio,Daniel G. Glaze,Gerald McGwin,Walter E. Kaufmann,Alan K. Percy,Jeffrey L. Neul,Michelle L. Olsen |
| Citations | 317 |
| DOI | 10.1136/jmedgenet-2013-102113 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | true |
| OA Status | bronze |
| OA URL | https://jmg.bmj.com/content/jmedgenet/51/3/152.full.pdf |
| OpenAlex ID | https://openalex.org/W2099517884 |
| PMID | 24399845 |
| Type | article |
| Year | 2014 |

## Paper authors

- [Daniel G. Glaze](https://scholariq.org/researchers/daniel-g-glaze/)
- [Gerald McGwin](https://scholariq.org/researchers/gerald-mcgwin/)

## Paper primary topic

- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

## Paper topics

- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Ubiquitin and proteasome pathways](https://scholariq.org/topics/ubiquitin-and-proteasome-pathways/)
- [Neurogenetic and Muscular Disorders Research](https://scholariq.org/topics/neurogenetic-and-muscular-disorders-research/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.