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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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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elsevier
2021
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| 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 |