Phenotypic heterogeneity of a compound heterozygous
SUCLA2
mutation
Mol Genet Metab Rep
.
2016 Dec 23:10:31-32.
doi: 10.1016/j.ymgmr.2016.12.007.
eCollection 2017 Mar.
Authors
Josef Finsterer
1
,
Sinda Zarrouk-Mahjoub
2
Affiliations
1
Krankenanstalt Rudolfstiftung, Vienna, Austria.
2
University of Tunis El Manar, Genomics Platform, Pasteur Institute of Tunis, Tunisia.
PMID:
28053875
PMCID:
PMC5198857
DOI:
10.1016/j.ymgmr.2016.12.007
No abstract available
Keywords:
Deafness; Diabetes; Gene; M.9155A > G; Mitochondrial disorder; Stroke-like episode; mtDNA.