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Mitochondrial DNA sequence variation in Finnish patients with matrilineal diabetes mellitus
BACKGROUND: The genetic background of type 2 diabetes is complex involving contribution by both nuclear and mitochondrial genes. There is an excess of maternal inheritance in patients with type 2 diabetes and, furthermore, diabetes is a common symptom in patients with mutations in mitochondrial DNA...
Kaydedildi:
| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2012
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3434112/ https://ncbi.nlm.nih.gov/pubmed/22780954 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1756-0500-5-350 |
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