Fuhrmann, N., Schimpf, S., Kamenisch, Y., Leo-Kottler, B., Alexander, C., Auburger, G., . . . Alavi, M. V. (2010). Solving a 50 year mystery of a missing OPA1 mutation: More insights from the first family diagnosed with autosomal dominant optic atrophy. BioMed Central.

Fuhrmann, Nico, Simone Schimpf, York Kamenisch, Beate Leo-Kottler, Christiane Alexander, Georg Auburger, Eberhart Zrenner, Bernd Wissinger, and Marcel V. Alavi. Solving a 50 Year Mystery of a Missing OPA1 Mutation: More Insights From the First Family Diagnosed With Autosomal Dominant Optic Atrophy. BioMed Central, 2010.

Fuhrmann, Nico, et al. Solving a 50 Year Mystery of a Missing OPA1 Mutation: More Insights From the First Family Diagnosed With Autosomal Dominant Optic Atrophy. BioMed Central, 2010.