The features of the m.10197G>A mtDNA mutation
J Neurol Sci
.
2019 May 15:400:184-185.
doi: 10.1016/j.jns.2019.04.005.
Epub 2019 Apr 4.
Authors
Mariasavina Severino
1
,
Claudia Nesti
2
,
Anna Rubegni
2
,
Deborah Tolomeo
3
,
Filippo M Santorelli
4
Affiliations
1
Neuroradiology Unit, Istituto Giannina Gaslini, Largo G. Gaslini 5, 16147 Genova, Italy. Electronic address: mariasavinaseverino@gaslini.org.
2
IRCCS Fondazione Stella Maris, viale del Tirreno 331, 56128 Calambrone, Pisa, Italy.
3
Department of Clinical and Experimental Medicine, University of Pisa, viale del Tirreno 331, 56128 Calambrone, Pisa, Italy. Electronic address: deborah.tolomeo@fsm.unipi.it.
4
IRCCS Fondazione Stella Maris, viale del Tirreno 331, 56128 Calambrone, Pisa, Italy. Electronic address: filippo3364@gmail.com.
PMID:
30978516
DOI:
10.1016/j.jns.2019.04.005
No abstract available
Keywords:
Leigh syndrome; MELAS; mtDNA.
Publication types
Letter
Comment
MeSH terms
DNA, Mitochondrial
Humans
Leigh Disease*
Mutation
Neuroimaging
Phenotype
Substances
DNA, Mitochondrial