A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration

Rett syndrome (RTT) is a rare neurological disorder mostly caused by a genetic variation in MECP2. Making new MECP2 variants and the related phenotypes available provides data for better understanding of disease mechanisms and faster identification of variants for diagnosis. This is, however, curren...

Descripción completa

Detalles Bibliográficos
Autores principales: Ehrhart, Friederike, Jacobsen, Annika, Rigau, Maria, Bosio, Mattia, Kaliyaperumal, Rajaram, Laros, Jeroen F. J., Willighagen, Egon L., Valencia, Alfonso, Roos, Marco, Capella-Gutierrez, Salvador, Curfs, Leopold M. G., Evelo, Chris T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Data Descriptor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7810705/
https://www.ncbi.nlm.nih.gov/pubmed/33452270
http://dx.doi.org/10.1038/s41597-020-00794-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7810705/
https://www.ncbi.nlm.nih.gov/pubmed/33452270
http://dx.doi.org/10.1038/s41597-020-00794-7

Ejemplares similares