Matches in SemOpenAlex for { <https://semopenalex.org/work/W1996881587> ?p ?o ?g. }
- W1996881587 endingPage "166" @default.
- W1996881587 startingPage "158" @default.
- W1996881587 abstract "Over the past 12 years, a wide variety of neurodegenerative diseases has been linked to mutations in mitochondrial genes located in either the mitochondrial DNA (mtDNA) or the nuclear DNA (nDNA). These disorders encompass an array of unorthodox inheritance patterns and a plethora of symptoms ranging from lethal neonatal multi-symptom disorders to later onset myopathies, cardiomyopathies, movement disorders, and dementias. The bases for the genetic and phenotypic variability of mitochondrial diseases lie in the multiplicity of the mitochondria genes dispersed across the human genome and the variety of cellular pathways and functions in which the mitochondria play a central role." @default.
- W1996881587 created "2016-06-24" @default.
- W1996881587 creator A5085274471 @default.
- W1996881587 date "2001-08-01" @default.
- W1996881587 modified "2023-10-16" @default.
- W1996881587 title "Mitochondrial defects in neurodegenerative disease" @default.
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