Only male matrilineal relatives with Leber’s hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation
- 1 March 2005
- journal article
- clinical trial
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 328 (4) , 1139-1145
- https://doi.org/10.1016/j.bbrc.2005.01.062
Abstract
No abstract availableKeywords
Funding Information
- Natural Science Foundation of Zhejiang Province (Z204492, ZB0202)
- National Institutes of Health (NS44015)
- National Institute of Neurological Disorders and Stroke
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