Mei, S., Huang, X., Cheng, L., Peng, S., Zhu, T., Chen, L., . . . Zhao, J. (2019). A Missense Mutation in OPA1 Causes Dominant Optic Atrophy in a Chinese Family. J Ophthalmol.
Chicago ZitierstilMei, Shaoyi, Xiaosheng Huang, Lin Cheng, Shiming Peng, Tianhui Zhu, Liang Chen, Yan Wang, und Jun Zhao. "A Missense Mutation in OPA1 Causes Dominant Optic Atrophy in a Chinese Family." J Ophthalmol 2019.
MLA ZitierstilMei, Shaoyi, et al. "A Missense Mutation in OPA1 Causes Dominant Optic Atrophy in a Chinese Family." J Ophthalmol 2019.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.