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Α rare case of myopathy, lactic acidosis, and severe rhabdo..:
Gkiourtzis, Nikolaos
;
Tramma, Despoina
;
Papadopoulou‐Legbelou, Kyriaki
..
American Journal of Medical Genetics Part A. 191 (2023) 12 - p. 2843-2849 , 2023
Link:
https://doi.org/10.1002/ajmg.a.63368
RT Journal T1
Α rare case of myopathy, lactic acidosis, and severe rhabdomyolysis, due to a homozygous mutation of the ferredoxin‐2 (FDX2) gene
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.a.63368&Exemplar=1&LAN=DE A1 Gkiourtzis, Nikolaos A1 Tramma, Despoina A1 Papadopoulou‐Legbelou, Kyriaki A1 Moutafi, Maria A1 Evangeliou, Athanasios PB Wiley YR 2023 SN 1552-4825 SN 1552-4833 JF American Journal of Medical Genetics Part A VO 191 IS 12 SP 2843 OP 2849 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.a.63368 DO https://doi.org/10.1002/ajmg.a.63368 SF ELIB - SuUB Bremen
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