Novel homozygous missense variants in MED27 associated with neurodevelopmental disorder: Clinical and pathogenetic research-Reference-Cited by-同舟云学术

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Novel homozygous missense variants in MED27 associated with neurodevelopmental disorder: Clinical and pathogenetic research

Published:2024-09 Issue:17 Volume:10 Page:e37258
ISSN:2405-8440
Container-title:Heliyon
language:en
Short-container-title:Heliyon

Author:

Wu Gongao,Lian Ruofei,Li Mengchun,Jin Liang,Jia Tianming,Wang Lijun,Gan Ling,Zhao Shichao,Liang Ruirui,Dong Yan^ORCID

Publisher

Elsevier BV

Reference17 articles.

1. MED27 variants cause developmental delay, dystonia, and cerebellar hypoplasia;Meng;Ann. Neurol.,2021

2. Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders;Maroofian;Brain,2023

3. The mediator complex: at the nexus of RNA polymerase II transcription;Jeronimo;Trends Cell Biol.,2017

4. The Mediator complex: a master coordinator of transcription and cell lineage development;Yin;Development,2014

5. Involvement of Mediator complex in malignancy;Schiano;Biochim. Biophys. Acta,2014

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