Precision medicine in diabetes: A non‐invasive prenatal diagnostic test for the determination of fetal glucokinase mutations

Hyperglycemia caused by mutations in the glucokinase gene, GCK, is the most common form of monogenic diabetes. Prenatal diagnosis is important, as it impacts on treatment. This study reports a monogenic non‐invasive prenatal diagnostic (NIPD‐M) test on cell‐free DNA in maternal plasma using the rela...

Descripción completa

Detalles Bibliográficos
Autores principales: Nouspikel, Thierry, Blouin, Jean‐Louis, Puder, Jardena J, Köhler Ballan, Bettina, Schwitzgebel, Valerie M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Short Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847152/
https://www.ncbi.nlm.nih.gov/pubmed/34469064
http://dx.doi.org/10.1111/jdi.13656

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847152/
https://www.ncbi.nlm.nih.gov/pubmed/34469064
http://dx.doi.org/10.1111/jdi.13656

Ejemplares similares