Cita APA

Schnieders, M. J., Goar, W., Griess, M., Roos, B. R., Scheetz, T. E., Stone, E. M., & Fingert, J. H. (2018). A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree. Eye (Lond).

Chicago Style Citation

Schnieders, M J., W. Goar, M. Griess, B R. Roos, T E. Scheetz, E M. Stone, i J H. Fingert. "A Novel Mutation (LEU396ARG) in OPA1 Is Associated With a Severe Phenotype in a Large Dominant Optic Atrophy Pedigree." Eye (Lond) 2018.

Cita MLA

Schnieders, M J., et al. "A Novel Mutation (LEU396ARG) in OPA1 Is Associated With a Severe Phenotype in a Large Dominant Optic Atrophy Pedigree." Eye (Lond) 2018.