Infantile-onset deafness in m.7445A>G carriers may be multicausal
Int J Pediatr Otorhinolaryngol
.
2018 Aug:111:192-193.
doi: 10.1016/j.ijporl.2018.06.024.
Epub 2018 Jun 14.
Authors
Josef Finsterer
1
,
Sinda Zarrouk-Mahjoub
2
Affiliations
1
Krankenanstalt Rudolfstiftung, Vienna, Austria. Electronic address: fifigs1@yahoo.de.
2
University of Tunis El Manar and Genomics Platform, Pasteur Institute of Tunis, Tunisia.
PMID:
29921456
DOI:
10.1016/j.ijporl.2018.06.024
No abstract available
Keywords:
Deafness; Hearing; Heterogeneity; Heteroplasmy; Mitochondrial; Multisystem; mtDNA.
Publication types
Letter
Comment
MeSH terms
DNA, Mitochondrial
Deafness*
Heterozygote*
Humans
Mutation
Substances
DNA, Mitochondrial