Do second generation sequencing techniques identify documented genetic markers for neonatal diabetes mellitus?

Neonatal diabetes mellitus (NDM) is noted as a genetic, heterogeneous, and rare disease in infants. NDM occurs due to a single-gene mutation in neonates. A common source for developing NDM in an infant is the existence of mutations/variants in the KCNJ11 and ABCC8 genes, encoding the subunits of the...

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Detalles Bibliográficos
Autor principal: Ali Khan, Imran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455689/
https://www.ncbi.nlm.nih.gov/pubmed/34584998
http://dx.doi.org/10.1016/j.heliyon.2021.e07903

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455689/
https://www.ncbi.nlm.nih.gov/pubmed/34584998
http://dx.doi.org/10.1016/j.heliyon.2021.e07903

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