@article{c913acb7e77f4c80ac91c958275b75cc,
title = "'Behr syndrome' with OPA1 compound heterozygote mutations",
abstract = "Not available",
keywords = "Central Nervous System Diseases, Female, GTP Phosphohydrolases, Humans, Male, Optic Atrophy, Autosomal Dominant, Central Nervous System Diseases, Female, GTP Phosphohydrolases, Humans, Male, Optic Atrophy, Autosomal Dominant",
author = "Mario Sabatelli and Bertini, {Enrico Silvio} and Valerio Carelli and Rosalba Carrozzo and Teresa Rizza and Simone Schimpf and Bernd Wissinger and Claudia Zanna and Michela Rugolo and {La Morgia}, Chiara and Leonardo Caporali and Michele Carbonelli and Piero Barboni and Caterina Tonon and Raffaele Lodi and Enrico Bertini",
year = "2015",
doi = "10.1093/brain/awu234",
language = "English",
volume = "138",
pages = "e321--e321",
journal = "Brain",
issn = "0006-8950",
publisher = "Oxford : Oxford University Press",
}