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Mutations in KCNJ11 are associated with the development of autosomal dominant, early-onset type 2 diabetes
AIMS/HYPOTHESIS: More than 90% of Chinese familial early-onset type 2 diabetes mellitus is genetically unexplained. To investigate the molecular aetiology, we identified and characterised whether mutations in the KCNJ11 gene are responsible for these families. METHODS: KCNJ11 mutations were screened...
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| Publicado no: | Diabetologia |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5333983/ https://ncbi.nlm.nih.gov/pubmed/24018988 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00125-013-3031-9 |
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