Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescence

INTRODUCTION: The mitochondrial DNA A3243G point mutation is associated with a wide variety of systemic manifestations including a macular dystrophy. The characteristics of fundus autofluorescence (AF) in these patients are distinctive and have not been previously described. METHODS: A complete hist...

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Detalles Bibliográficos
Autores principales: Rath, P P, Jenkins, S, Michaelides, M, Smith, A, Sweeney, M G, Davis, M B, Fitzke, F W, Bird, A C
Formato: Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2008
Materias:
Clinical Science
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2569141/
https://www.ncbi.nlm.nih.gov/pubmed/18441172
http://dx.doi.org/10.1136/bjo.2007.131177

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2569141/
https://www.ncbi.nlm.nih.gov/pubmed/18441172
http://dx.doi.org/10.1136/bjo.2007.131177

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