Severe manifestation of Leber's hereditary optic neuropathy due to 11778G>A mtDNA mutation in a female with hypoestrogenism due to Perrault syndrome. [electronic resource]
Producer: 20140715Description: 831-4 p. digitalISSN:- 1872-8278
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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