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1 Ergebnisse
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Case Report: Rare Homozygous RNASEH1 Mutations Associated W..:
Manini, Arianna
;
Caporali, Leonardo
;
Meneri, Megi
...
info:eu-repo/semantics/altIdentifier/pmid/35711919. , 2022
Link:
https://hdl.handle.net/11585/903061
RT Journal T1
Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions
UL https://suche.suub.uni-bremen.de/peid=base-ftunibolognairis:oai:cris.unibo.it:11585_903061&Exemplar=1&LAN=DE A1 Manini, Arianna A1 Caporali, Leonardo A1 Meneri, Megi A1 Zanotti, Simona A1 Piga, Daniela A1 Arena, Ignazio Giuseppe A1 Corti, Stefania A1 Toscano, Antonio A1 Comi, Giacomo Pietro A1 Musumeci, Olimpia A1 Carelli, Valerio A1 Ronchi, Dario YR 2022 K1 CPEO K1 RNASEH1 K1 mitochondrial DNA K1 mtDNA maintenance disorder K1 myopathy K1 ribonuclease H1 JF info:eu-repo/semantics/altIdentifier/pmid/35711919 LK http://dx.doi.org/https://hdl.handle.net/11585/903061 DO https://hdl.handle.net/11585/903061 SF ELIB - SuUB Bremen
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