@article{c913acb7e77f4c80ac91c958275b75cc,
title = "'Behr syndrome' with OPA1 compound heterozygote mutations",
abstract = "Not available",
keywords = "Autosomal Dominant, Central Nervous System Diseases, Female, GTP Phosphohydrolases, Humans, Male, Optic Atrophy, Autosomal Dominant, Central Nervous System Diseases, Female, GTP Phosphohydrolases, Humans, Male, Optic Atrophy",
author = "V. Carelli and Mario Sabatelli and R. Carrozzo and T. Rizza and S. Schimpf and B. Wissinger and C. Zanna and M. Rugolo and La, \{Morgia C.\} and L. Caporali and M. Carbonelli and P. Barboni and C. Tonon and R. Lodi and E. Bertini",
year = "2015",
doi = "10.1093/brain/awu234",
language = "English",
volume = "138",
pages = "e321--e321",
journal = "Brain",
issn = "0006-8950",
publisher = "United Kingdom, Oxford : Oxford University Press",
number = "Pt 1",
}