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Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders
MED27 is a subunit of the Mediator multiprotein complex, which is involved in transcriptional regulation. Biallelic MED27 variants have recently been suggested to be responsible for an autosomal recessive neurodevelopmental disorder with spasticity, cataracts and cerebellar hypoplasia. We further de...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690011/ https://www.ncbi.nlm.nih.gov/pubmed/37517035 http://dx.doi.org/10.1093/brain/awad257 |