![](/img/cover-not-exists.png)
Pure and syndromic optic atrophy explained by deep intronic OPA1 mutations and an intralocus modifier
Bonifert, T., Karle, K. N., Tonagel, F., Batra, M., Wilhelm, C., Theurer, Y., Schoenfeld, C., Kluba, T., Kamenisch, Y., Carelli, V., Wolf, J., Gonzalez, M. A., Speziani, F., Schule, R., Zuchner, S., SVolume:
137
Language:
english
Journal:
Brain
DOI:
10.1093/brain/awu165
Date:
August, 2014
File:
PDF, 1.23 MB
english, 2014