'Behr syndrome' with OPA1 compound heterozygote mutations

Valerio Carelli, Mario Sabatelli, Rosalba Carrozzo, Teresa Rizza, Simone Schimpf, Bernd Wissinger, Claudia Zanna, Michela Rugolo, Chiara La Morgia, Leonardo Caporali, Michele Carbonelli, Piero Barboni, Caterina Tonon, Raffaele Lodi, Enrico Bertini

Research output: Contribution to journalArticle

19 Citations (Scopus)
Original languageEnglish
Pages (from-to)e321
JournalBrain
Volume138
DOIs
Publication statusPublished - Jan 1 2015

ASJC Scopus subject areas

  • Medicine(all)

Cite this

'Behr syndrome' with OPA1 compound heterozygote mutations. / Carelli, Valerio; Sabatelli, Mario; Carrozzo, Rosalba; Rizza, Teresa; Schimpf, Simone; Wissinger, Bernd; Zanna, Claudia; Rugolo, Michela; La Morgia, Chiara; Caporali, Leonardo; Carbonelli, Michele; Barboni, Piero; Tonon, Caterina; Lodi, Raffaele; Bertini, Enrico.

In: Brain, Vol. 138, 01.01.2015, p. e321.

Research output: Contribution to journalArticle

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 2015, ''Behr syndrome' with OPA1 compound heterozygote mutations', Brain, vol. 138, pp. e321. https://doi.org/10.1093/brain/awu234
Carelli, Valerio ; Sabatelli, Mario ; Carrozzo, Rosalba ; Rizza, Teresa ; Schimpf, Simone ; Wissinger, Bernd ; Zanna, Claudia ; Rugolo, Michela ; La Morgia, Chiara ; Caporali, Leonardo ; Carbonelli, Michele ; Barboni, Piero ; Tonon, Caterina ; Lodi, Raffaele ; Bertini, Enrico. / 'Behr syndrome' with OPA1 compound heterozygote mutations. In: Brain. 2015 ; Vol. 138. pp. e321.
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