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1 Ergebnisse
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UQCRC2 mutation in a patient with mitochondrial complex III..:
Gaignard, Pauline
;
Eyer, Didier
;
Lebigot, Elise
...
Journal of Human Genetics. 62 (2017) 7 - p. 729-731 , 2017
Link:
https://doi.org/10.1038/jhg.2017.22
RT Journal T1
UQCRC2 mutation in a patient with mitochondrial complex III deficiency causing recurrent liver failure, lactic acidosis and hypoglycemia
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_jhg.2017.22&Exemplar=1&LAN=DE A1 Gaignard, Pauline A1 Eyer, Didier A1 Lebigot, Elise A1 Oliveira, Christophe A1 Therond, Patrice A1 Boutron, Audrey A1 Slama, Abdelhamid PB Springer Science and Business Media LLC YR 2017 SN 1434-5161 SN 1435-232X JF Journal of Human Genetics VO 62 IS 7 SP 729 OP 731 LK http://dx.doi.org/https://doi.org/10.1038/jhg.2017.22 DO https://doi.org/10.1038/jhg.2017.22 SF ELIB - SuUB Bremen
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