Open AccessCombination of common mtDNA variants results in mitochondrial dysfunction and a connective tissue dysregulation
Author(s) -
Patrick Schaefer,
Leonardo Scherer Alves,
Maria Lvova,
Jessica Huang,
Komal S. Rathi,
Kevin A. Janssen,
Arrienne Butic,
Tal Yardeni,
Ryan Morrow,
Marie T. Lott,
Deborah G. Murdock,
Angela Song,
Kierstin Keller,
Benjamin A. García,
Clair A. Francomano,
Douglas C. Wallace
Publication year - 2022
Publication title -
proceedings of the national academy of sciences of the united states of america
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.2212417119
Subject(s) - mitochondrial dna , biology , haplogroup , genetics , mitochondrion , human mitochondrial dna haplogroup , mitochondrial disease , allele , genotype , gene , haplotype