TY  - GEN
AU  - Züchner,Stephan
AU  - De Jonghe,Peter
AU  - Jordanova,Albena
AU  - Claeys,Kristl G
AU  - Guergueltcheva,Velina
AU  - Cherninkova,Sylvia
AU  - Hamilton,Steven R
AU  - Van Stavern,Greg
AU  - Krajewski,Karen M
AU  - Stajich,Jeffery
AU  - Tournev,Ivajlo
AU  - Verhoeven,Kristien
AU  - Langerhorst,Christine T
AU  - de Visser,Marianne
AU  - Baas,Frank
AU  - Bird,Thomas
AU  - Timmerman,Vincent
AU  - Shy,Michael
AU  - Vance,Jeffery M
TI  - Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2
SN  - 0364-5134
PY  - 2006///0425
KW  - Adolescent
KW  - Adult
KW  - Age of Onset
KW  - Charcot-Marie-Tooth Disease
KW  - complications
KW  - Child
KW  - DNA Mutational Analysis
KW  - methods
KW  - Family Health
KW  - GTP Phosphohydrolases
KW  - Genetic Predisposition to Disease
KW  - genetics
KW  - Humans
KW  - Membrane Proteins
KW  - Middle Aged
KW  - Mitochondrial Proteins
KW  - Models, Biological
KW  - Mutation
KW  - Neural Conduction
KW  - physiology
KW  - Optic Atrophy
KW  - etiology
KW  - Pedigree
KW  - Visual Acuity
N1  - Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ana.20797
ER  -