NDUFA2 - Associated Mitochondrial Disorder Requires Thorough Clinical and Genetic Work-Up in First-Degree Family Members
Josef Finsterer *
Krankenanstalt Rudolfstiftung, Vienna, Austria
Sinda Zarrouk-Mahjoub
University of Tunis El Manar and Genomics Platform, Pasteur Institute of Tunis, Tunisia
*Author to whom correspondence should be addressed.
Abstract
The “Type of Article” of this paper is “Letter to the Editor”. This paper discuses about: “NDUFA2 - Associated Mitochondrial Disorder Requires Thorough Clinical and Genetic Work-Up in First-Degree Family Members”. No formal abstract is available. Readers are requested to read the full article.
Keywords: Mitochondrial, mtDNA, leigh syndrome, cerebal, cardiomyopathy