Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy

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Nonsyndromic sensorineural deafness associated with the A1555G mutation in the mitochondrial small subunit ribosomal RNA in a Balinese family
Evidence for the de novo regeneration of the pattern of the length heteroplasmy associated with the T16189C variant in the control (D-loop) region of mitochondrial DNA
Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy
The unique characteristics of Thai Leber hereditary optic neuropathy : analysis of 30 G11778A pedigrees
Leber's Hereditary Optic Neuropathy in Thailand
Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia
The Hemoglobin O mutation in Indonesia : distribution and phenotypic expression
An Unusual Electrophysiologic Finding in Acute Stage of Leber's Hereditary Optic Neuropathy
Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy
Molecular population genetics of SLC4A1 and Southeast Asian Ovalocytosis
Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages

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