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The phenotype modifier: is the mitochondrial DNA background responsible for individual differences in disease severity
Author(s) -
Morava Eva,
Kozicz Tamas,
Wallace Douglas C
Publication year - 2019
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1002/jimd.12050
Subject(s) - haplogroup , mitochondrial dna , genetics , biology , human mitochondrial dna haplogroup , penetrance , human mitochondrial genetics , phenotype , mitochondrial disease , population , gene , human genetics , mitochondrion , nuclear gene , haplotype , allele , medicine , environmental health
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