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Two sisters with macular dystrophy caused by the 3243A>G mitochondrial DNA mutation

V Sánchez-Gutiérrez1, J García-Montesinos1, A Pardo-Muñoz1

  • 1Departamento de Oftalmología, Hospital Universitario Ramón y Cajal, Madrid, España.

Archivos De La Sociedad Espanola De Oftalmologia
|February 22, 2016
PubMed
Abstract

Keywords:
ADN mitocondrialBallinger-Wallace syndromeDeafnessDiabetesDistrofia macularEnfermedad mitocondrialMacular dystrophyMitochondrial DNAMitochondrial diseaseSorderaSíndrome de Ballinger-Wallace

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