Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome

BACKGROUND: Mitochondrial disorders are clinically complex and have highly variable phenotypes among all inherited disorders. Mutations in mitochon drial DNA (mtDNA) and nuclear genome or both have been reported in mitochondrial diseases suggesting common pathophysiological pathways. Considering the...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Neurol
Egile Nagusiak: Chakrabarty, Sanjiban, Govindaraj, Periyasamy, Sankaran, Bindu Parayil, Nagappa, Madhu, Kabekkodu, Shama Prasada, Jayaram, Pradyumna, Mallya, Sandeep, Deepha, Sekar, Ponmalar, J. N. Jessiena, Arivinda, Hanumanthapura R., Meena, Angamuthu Kanikannan, Jha, Rajan Kumar, Sinha, Sanjib, Gayathri, Narayanappa, Taly, Arun B., Thangaraj, Kumarasamy, Satyamoorthy, Kapaettu
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Springer Berlin Heidelberg 2021
Gaiak:
Original Communication
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC8179915/
https://ncbi.nlm.nih.gov/pubmed/33484326
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00415-020-10390-9
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