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Homozygous missense mutation in UQCRC2 associated with seve..:
Burska, Daniela
;
Stiburek, Lukas
;
Krizova, Jana
...
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1867 (2021) 8 - p. 166147 , 2021
Link:
https://doi.org/10.1016/j.bbadis.2021.166147
RT Journal T1
Homozygous missense mutation in UQCRC2 associated with severe encephalomyopathy, mitochondrial complex III assembly defect and activation of mitochondrial protein quality control
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.bbadis.2021.166147&Exemplar=1&LAN=DE A1 Burska, Daniela A1 Stiburek, Lukas A1 Krizova, Jana A1 Vanisova, Marie A1 Martinek, Vaclav A1 Sladkova, Jana A1 Zamecnik, Josef A1 Honzik, Tomas A1 Zeman, Jiri A1 Hansikova, Hana A1 Tesarova, Marketa PB Elsevier BV YR 2021 SN 0925-4439 JF Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease VO 1867 IS 8 SP 166147 LK http://dx.doi.org/https://doi.org/10.1016/j.bbadis.2021.166147 DO https://doi.org/10.1016/j.bbadis.2021.166147 SF ELIB - SuUB Bremen
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