
Polymorphism of the clinical manifestations of progressive mitochondrial encephalomyopathy associated with POLG1 gene mutation
Author(s) -
М И Яблонская,
Е. А. Николаева,
P.A. Shatalov,
М. Н. Харабадзе
Publication year - 2016
Publication title -
rossijskij vestnik perinatologii i pediatrii
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.139
H-Index - 4
eISSN - 2500-2228
pISSN - 1027-4065
DOI - 10.21508/1027-4065-2016-61-3-51-57
Subject(s) - mitochondrial dna , genetics , biology , gene , mutation , polymerase , phenotype , gene mutation