Lookup NU author(s): Dr Yi Ng,
Dr Patrick Yu Wai Man,
Professor Robert Taylor
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Maternally inherited mitochondrial DNA (mtDNA) mutations cause symptoms of Leber hereditary optic neuropathy (LHON) in approximate to 1 in 30,000 individuals. Most of the affected individuals lack respiratory chain defects(1) and there is no proven prophylactic treatment.
Author(s): Dombi E, Diot A, Morten K, Carver J, Lodge T, Fratter C, Ng YS, Liao CY, Muir R, Blakely EL, Hargreaves I, Al-Dosary M, Sarkar G, Hickman SJ, Downes SM, Jayawant S, Yu-Wai-Man P, Taylor RW, Poulton J
Publication type: Editorial
Publication status: Published
Print publication date: 17/05/2016
Online publication date: 22/04/2016
Acceptance date: 25/01/2016
ISSN (print): 0028-3878
ISSN (electronic): 1526-632X
Publisher: Lippincott Williams & Wilkins