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Secondary manifestations of mitochondrial disorders

Mitochondrial disorders (MIDs) are a heterogeneous group of genetic metabolic diseases due to mutations in the mitochondrial DNA (mtDNA) or in the nuclear DNA (nDNA) (Rahman and Rahman, 2018). Some affected genes encode proteins with various functions, or structural RNAs such as transfer RNAs (tRNAs...

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Bibliografske podrobnosti
izdano v:J Zhejiang Univ Sci B
Glavni avtor: Finsterer, Josef
Format: Artigo
Jezik:Inglês
Izdano: Zhejiang University Press 2020
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7383320/
https://ncbi.nlm.nih.gov/pubmed/32633113
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1631/jzus.B2000010
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