APA

Fuhrmann N., Schimpf S., Kamenisch Y., Leo-Kottler B., Alexander C., Auburger G., Zrenner E., Wissinger B. & Alavi M. V. (20110714). Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy. : Molecular neurodegeneration.

Chicago

Fuhrmann Nico, Schimpf Simone, Kamenisch York, Leo-Kottler Beate, Alexander Christiane, Auburger Georg, Zrenner Eberhart, Wissinger Bernd and Alavi Marcel V. 20110714. Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy. : Molecular neurodegeneration.

Harvard

Fuhrmann N., Schimpf S., Kamenisch Y., Leo-Kottler B., Alexander C., Auburger G., Zrenner E., Wissinger B. and Alavi M. V. (20110714). Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy. : Molecular neurodegeneration.

MLA

Fuhrmann Nico, Schimpf Simone, Kamenisch York, Leo-Kottler Beate, Alexander Christiane, Auburger Georg, Zrenner Eberhart, Wissinger Bernd and Alavi Marcel V. Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy. : Molecular neurodegeneration. 20110714.