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Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6888 individuals
BACKGROUND: Diagnosis of monogenic as well as atypical forms of diabetes mellitus has important clinical implications for their specific diagnosis, prognosis, and targeted treatment. Single gene mutations that affect beta-cell function represent 1–2% of all cases of diabetes. However, phenotypic het...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717832/ https://www.ncbi.nlm.nih.gov/pubmed/29207974 http://dx.doi.org/10.1186/s12916-017-0977-3 |