Sindrome da deplezione del DNA mitocondriale (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sindrome da deplezione del DNA mitocondriale" in Italian language version.

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Mitochondrial DNA Depletion Syndromes: Review and Updates of Genetic Basis, Manifestations, and Therapeutic Options, vol. 10, DOI:10.1007/s13311-013-0177-6, PMID 23385875.
Deoxyribonucleotides and disorders of mitochondrial DNA integrity, vol. 23, DOI:10.1089/dna.2004.23.797, PMID 15684706.
Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletion, vol. 76, DOI:10.1086/430843, PMID 15877282.
Defects in mitochondrial DNA replication and human disease, vol. 47, DOI:10.3109/10409238.2011.632763, PMID 22176657.
Molecular insight into mitochondrial DNA depletion syndrome in two patients with novel mutations in the deoxyguanosine kinase and thymidine kinase 2 genes, vol. 84, DOI:10.1016/j.ymgme.2004.09.005, PMID 15639197.
Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions, vol. 28, DOI:10.1038/90034, PMID 11431686.
Abnormal neurological features predict poor survival and should preclude liver transplantation in patients with deoxyguanosine kinase deficiency, vol. 14, DOI:10.1002/lt.21556, PMID 18825706.
MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: New patients and novel mutations, vol. 99, DOI:10.1016/j.ymgme.2009.10.003, PMID 20074988.
Emerging concepts in the therapy of mitochondrial disease, vol. 1847, DOI:10.1016/j.bbabio.2015.03.001, PMID 25766847.
Feeding the deoxyribonucleoside salvage pathway to rescue mitochondrial DNA, vol. 18, DOI:10.1016/j.drudis.2013.06.009, PMID 23817075.

nih.gov

ncbi.nlm.nih.gov

ninds.nih.gov

Alpers' Disease Information Page, su ninds.nih.gov.

oadoi.org

omim.org

web.archive.org

Copia archiviata, su labor-lademannbogen.de. URL consultato il 31 luglio 2017 (archiviato dall'url originale il 26 gennaio 2022).