Detecting AGG Interruptions in Females With a FMR1 Premutation by Long-Read Single-Molecule Sequencing: A 1 Year Clinical Experience

The fragile X syndrome arises from the FMR1 CGG expansion of a premutation (55–200 repeats) to a full mutation allele (>200 repeats) and is the most frequent cause of inherited X-linked intellectual disability. The risk for a premutation to expand to a full mutation allele depends on the repeat l...

Descripción completa

Detalles Bibliográficos
Autores principales: Ardui, Simon, Race, Valerie, de Ravel, Thomy, Van Esch, Hilde, Devriendt, Koenraad, Matthijs, Gert, Vermeesch, Joris R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964127/
https://www.ncbi.nlm.nih.gov/pubmed/29868108
http://dx.doi.org/10.3389/fgene.2018.00150

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964127/
https://www.ncbi.nlm.nih.gov/pubmed/29868108
http://dx.doi.org/10.3389/fgene.2018.00150

Ejemplares similares