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1 Ergebnisse
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A novel mitochondrial mutation m.8989G>C associated with ne..:
Duno, Morten
;
Wibrand, Flemming
;
Baggesen, Kirsten
...
https://vbn.aau.dk/da/publications/bf291774-b19c-4c81-ba40-5b53202011b6. , 2013
Link:
https://vbn.aau.dk/da/publications/bf291774-b19c-4c81-..
RT Journal T1
A novel mitochondrial mutation m.8989G>C associated with neuropathy, ataxia, retinitis pigmentosa - the NARP syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftalborgunivpubl:oai:pure.atira.dk:publications_bf291774-b19c-4c81-ba40-5b53202011b6&Exemplar=1&LAN=DE A1 Duno, Morten A1 Wibrand, Flemming A1 Baggesen, Kirsten A1 Rosenberg, Niels Thomas A1 Olsen, Niels Kjær A1 Frederiksen, Anja Lisbeth YR 2013 K1 Base Sequence K1 DNA Mutational Analysis K1 Genetic Association Studies K1 Humans K1 Male K1 Middle Aged K1 Mitochondria K1 Muscle K1 Mitochondrial Myopathies K1 Mitochondrial Proton-Translocating ATPases K1 Mutation K1 Missense K1 Retinitis Pigmentosa JF https://vbn.aau.dk/da/publications/bf291774-b19c-4c81-ba40-5b53202011b6 LK http://dx.doi.org/https://vbn.aau.dk/da/publications/bf291774-b19c-4c81-ba40-5b53202011b6 DO https://vbn.aau.dk/da/publications/bf291774-b19c-4c81-ba40-5b53202011b6 SF ELIB - SuUB Bremen
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