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Not only dominant, not only optic atrophy: expanding the cl..:

Nasca, Alessia ; Rizza, Teresa ; Doimo, Mara...
info:eu-repo/semantics/altIdentifier/pmid/28494813. , 2017

Link: http://hdl.handle.net/10281/205499

RT Journal
T1 <Title>Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftunivmilanobic:oai:boa.unimib.it:10281_205499&Exemplar=1&LAN=DE
				
A1 Nasca, Alessia
A1 Rizza, Teresa
A1 Doimo, Mara
A1 Legati, Andrea
A1 Ciolfi, Andrea
A1 Diodato, Daria
A1 Calderan, Cristina
A1 Carrara, Gianfranco
A1 Lamantea, Eleonora
A1 Aiello, Chiara
A1 Di Nottia, Michela
A1 Niceta, Marcello
A1 Lamperti, Costanza
A1 Ardissone, Anna
A1 Bianchi-Marzoli, Stefania
A1 Iarossi, Giancarlo
A1 Bertini, Enrico
A1 Moroni, Isabella
A1 Tartaglia, Marco
A1 Salviati, Leonardo
A1 Carrozzo, Rosalba
A1 Ghezzi, Daniele
PB BioMed Central Ltd.
YR 2017
K1 Encephalopathy
K1 Mitochondrial disorder
K1 OPA1
K1 Optic atrophy
K1 Recessive trait
K1 Targeted resequencing
K1 WES
K1 Blotting
K1 Western
K1 Brain Disease
K1 Child
K1 Preschool
K1 Electrophysiology
K1 GTP Phosphohydrolase
K1 Human
K1 Infant
K1 Male
K1 Microscopy
K1 Fluorescence
K1 Mutation
K1 Autosomal Dominant
K1 Tomography
K1 Optical Coherence
K1 Whole Exome Sequencing
K1 Genetics (clinical)
K1 Pharmacology (medical)
JF info:eu-repo/semantics/altIdentifier/pmid/28494813
LK http://hdl.handle.net/10281/205499
DO http://hdl.handle.net/10281/205499
SF ELIB - SuUB Bremen

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