Heteroplasmy levels of a mitochondrial g
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Leen M. 't Hart; Janna J. Jansen; Herman H.P.J. Lemkes; Peter de Knijff; J. Anto
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Article
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1996
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John Wiley and Sons
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English
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We showed previously that a mutation in the mitochondria1 tRNAL"(UUR' gene at position 3243 associates with maternally inherited diabetes and deafness (MIDD). This mutation shows heteroplasmy in DNA from peripheral blood and other tissues. To examine whether heteroplasmy levels in peripheral blood D