UQCRC2 mutation in a patient with mitochondrial complex III deficiency causing recurrent liver failure, lactic acidosis and hypoglycemia.
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UQCRC2 mutation in a patient with mitochondrial complex III deficiency causing recurrent liver failure, lactic acidosis and hypoglycemia.
description
2017 nî lūn-bûn
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name
UQCRC2 mutation in a patient w ...... tic acidosis and hypoglycemia.
@en
UQCRC2 mutation in a patient w ...... tic acidosis and hypoglycemia.
@nl
type
label
UQCRC2 mutation in a patient w ...... tic acidosis and hypoglycemia.
@en
UQCRC2 mutation in a patient w ...... tic acidosis and hypoglycemia.
@nl
prefLabel
UQCRC2 mutation in a patient w ...... tic acidosis and hypoglycemia.
@en
UQCRC2 mutation in a patient w ...... tic acidosis and hypoglycemia.
@nl
P2093
P2860
P356
P1476
UQCRC2 mutation in a patient w ...... ctic acidosis and hypoglycemia
@en
P2093
Abdelhamid Slama
Audrey Boutron
Christophe Oliveira
Didier Eyer
Elise Lebigot
Patrice Therond
P2860
P2888
P304
P356
10.1038/JHG.2017.22
P577
2017-03-09T00:00:00Z