TY  - GEN
AU  - Caporali,Leonardo
AU  - Iommarini,Luisa
AU  - La Morgia,Chiara
AU  - Olivieri,Anna
AU  - Achilli,Alessandro
AU  - Maresca,Alessandra
AU  - Valentino,Maria Lucia
AU  - Capristo,Mariantonietta
AU  - Tagliavini,Francesca
AU  - Del Dotto,Valentina
AU  - Zanna,Claudia
AU  - Liguori,Rocco
AU  - Barboni,Piero
AU  - Carbonelli,Michele
AU  - Cocetta,Veronica
AU  - Montopoli,Monica
AU  - Martinuzzi,Andrea
AU  - Cenacchi,Giovanna
AU  - De Michele,Giuseppe
AU  - Testa,Francesco
AU  - Nesti,Anna
AU  - Simonelli,Francesca
AU  - Porcelli,Anna Maria
AU  - Torroni,Antonio
AU  - Carelli,Valerio
TI  - Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy
SN  - 1553-7404
PY  - 2018///0718
KW  - Adult
KW  - Amino Acid Sequence
KW  - DNA, Mitochondrial
KW  - genetics
KW  - Electron Transport Complex I
KW  - chemistry
KW  - Epistasis, Genetic
KW  - Family
KW  - Female
KW  - Genes, Mitochondrial
KW  - Humans
KW  - Male
KW  - Models, Molecular
KW  - Multifactorial Inheritance
KW  - Mutation, Missense
KW  - NADH Dehydrogenase
KW  - Optic Atrophy, Hereditary, Leber
KW  - Pedigree
KW  - Penetrance
KW  - Young Adult
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1371/journal.pgen.1007210
ER  -