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Evaluation of a Mitochondrial DNA Mutation in Maternally Inherited and Sporadic Cases of Dupuytren Disease
OBJECTIVE: The purpose was to test the hypothesis that Dupuytren disease (DD) is associated with a previously reported mutation in mitochondrial DNA at position 2839. METHODS: Two hundred sixty-nine cases of DD and an equal number of matched controls were identified in Marshfield Clinic’s Personaliz...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Marshfield Clinic
2012
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3421422/ https://ncbi.nlm.nih.gov/pubmed/22634541 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3121/cmr.2012.1063 |
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