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'Behr syndrome' with OPA1 compound heterozygote mutations
Carelli, V., Sabatelli, M., Carrozzo, R., Rizza, T., Schimpf, S., Wissinger, B., Zanna, C., Rugolo, M., La Morgia, C., Caporali, L., Carbonelli, M., Barboni, P., Tonon, C., Lodi, R., Bertini, E.Volume:
138
Language:
english
Journal:
Brain
DOI:
10.1093/brain/awu234
Date:
January, 2015
File:
PDF, 841 KB
english, 2015