Pages that link to "Q33728325"
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The following pages link to Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C (Q33728325):
Displaying 13 items.
- Mitochondrial disorders and the eye. (Q33702120) (← links)
- Is mitochondrial tRNA(phe) variant m.593T>C a synergistically pathogenic mutation in Chinese LHON families with m.11778G>A? (Q34062474) (← links)
- Mitochondrial DNA haplogroup background affects LHON, but not suspected LHON, in Chinese patients (Q34081807) (← links)
- The case for the continuing use of the revised Cambridge Reference Sequence (rCRS) and the standardization of notation in human mitochondrial DNA studies (Q34389694) (← links)
- Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients (Q36023873) (← links)
- Physiology and pathophysiology of mitochondrial DNA. (Q36444799) (← links)
- Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>A and Leber hereditary optic neuropathy (Q36511591) (← links)
- Mitochondrial DNA haplogroup confers genetic susceptibility to nasopharyngeal carcinoma in Chaoshanese from Guangdong, China. (Q37539168) (← links)
- Pan-American mDNA haplogroups in Chilean patients with Leber's hereditary optic neuropathy (Q37656235) (← links)
- Leber Hereditary Optic Neuropathy: A Mitochondrial Disease Unique in Many Ways (Q40511873) (← links)
- Searching the co-occurrence of pathogenic mutations for Leber's hereditary optic neuropathy and hearing loss in more than 26,000 whole mitochondrial genomes (Q47434746) (← links)
- Association of mitochondrial haplogroup F with physical performance in Korean population (Q64098770) (← links)
- Contribution of Mitochondrial DNA Variation to Chronic Disease in East Asian Populations (Q91712161) (← links)