Clinical Heterogeneity and Different Phenotypes in Patients with SETD2 Variants: 18 New Patients and Review of the Literature

SETD2 belongs to the family of histone methyltransferase proteins and has been associated with three nosologically distinct entities with different clinical and molecular features: Luscan–Lumish syndrome (LLS), intellectual developmental disorder, autosomal dominant 70 (MRD70), and Rabin–Pappas synd...

Descripción completa

Detalles Bibliográficos
Autores principales: Parra, Alejandro, Rabin, Rachel, Pappas, John, Pascual, Patricia, Cazalla, Mario, Arias, Pedro, Gallego-Zazo, Natalia, Santana, Alfredo, Arroyo, Ignacio, Artigas, Mercè, Pachajoa, Harry, Alanay, Yasemin, Akgun-Dogan, Ozlem, Ruaud, Lyse, Couque, Nathalie, Levy, Jonathan, Porras-Hurtado, Gloria Liliana, Santos-Simarro, Fernando, Ballesta-Martinez, Maria Juliana, Guillén-Navarro, Encarna, Muñoz-Hernández, Hugo, Nevado, Julián, Tenorio-Castano, Jair, Lapunzina, Pablo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297832/
https://www.ncbi.nlm.nih.gov/pubmed/37372360
http://dx.doi.org/10.3390/genes14061179

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297832/
https://www.ncbi.nlm.nih.gov/pubmed/37372360
http://dx.doi.org/10.3390/genes14061179

Ejemplares similares