Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy

Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy

Abstract:

Citation:

  • Khan, N.A., Govindaraj, P., Jyothi, V., Meena, A.K. and Thangaraj, K. (2013). Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy. Molecular vision, 19, 1282.

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Keywords

Peoples: | Places: | Topics: | DNA Type: mtDNA

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