Diagnosing MELAS requires not only an mtDNA variant but also an appropriate phenotype
Doc Ophthalmol
.
2019 Jun;138(3):255-256.
doi: 10.1007/s10633-019-09690-x.
Epub 2019 Mar 28.
Authors
Josef Finsterer
1
,
Sinda Zarrouk-Mahjoub
2
Affiliations
1
Krankenanstalt Rudolfstiftung, Postfach 20, 1180, Vienna, Austria. fifigs1@yahoo.de.
2
Pasteur Institute of Tunis, University of Tunis El Manar and Genomics Platform, Tunis, Tunisia.
PMID:
30924003
DOI:
10.1007/s10633-019-09690-x
No abstract available
Publication types
Letter
Comment
MeSH terms
DNA, Mitochondrial
Electroretinography
Humans
MELAS Syndrome / genetics*
Phenotype
Retinal Dystrophies*
Sequence Deletion
Substances
DNA, Mitochondrial