# Autosomal dominant intellectual disability associated with the MED13L gene

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/autosomal-dominant-intellectual-disability-associated-with-the-med13l-gene/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Olga Levchenko,G. E. Rudenskaya,Т. В. Маркова,Л. А. Бессонова,Andrey V. Marakhonov,S. E. Nagieva,Olga Shchagina,А. В. Лавров |
| Citations | 1 |
| DOI | 10.21508/1027-4065-2022-67-1-101-107 |
| Fields | Biochemistry, Genetics and Molecular Biology |
| Open Access | true |
| OA Status | diamond |
| OA URL | https://doi.org/10.21508/1027-4065-2022-67-1-101-107 |
| OpenAlex ID | https://openalex.org/W4223544827 |
| Type | article |
| Year | 2022 |

## Paper authors

- [S. E. Nagieva](https://scholariq.org/researchers/s-e-nagieva/)

## Paper journal

- [Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics)](https://scholariq.org/journals/rossiyskiy-vestnik-perinatologii-i-pediatrii-russian-bulletin-of-perinatology/)

## 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/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)

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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.