MED12 Mutation in Two Families with X-Linked Ohdo Syndrome

X-linked intellectual deficiency (XLID) is a widely heterogeneous group of genetic disorders that involves more than 100 genes. The mediator of RNA polymerase II subunit 12 (MED12) is involved in the regulation of the majority of RNA polymerase II-dependent genes and has been shown to cause several...

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Detalles Bibliográficos
Autores principales: Rocchetti, Luca, Evangelista, Eloisa, De Falco, Luigia, Savarese, Giovanni, Savarese, Pasquale, Ruggiero, Raffaella, D’Amore, Luigi, Sensi, Alberto, Fico, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8471817/
https://www.ncbi.nlm.nih.gov/pubmed/34573309
http://dx.doi.org/10.3390/genes12091328

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8471817/
https://www.ncbi.nlm.nih.gov/pubmed/34573309
http://dx.doi.org/10.3390/genes12091328

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