Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy. [electronic resource]

By: Contributor(s): Producer: 20030122Description: 594-604 p. digitalISSN:
  • 1434-5161
Subject(s): Online resources: In: Journal of human genetics vol. 47
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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