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Recurrent acute liver failure and mitochondriopathy in a case of Wolcott–Rallison syndrome
by
Engelmann, G.
,
Meyburg, J.
,
Shahbek, N.
,
Al-Ali, M.
,
Hairetis, M. H.
,
Baker, A. J.
,
Rodenburg, R. J. T.
,
Wenning, D.
,
Flechtenmacher, C.
,
Ellard, S.
,
Smeitink, J. A.
,
Hoffmann, G. F.
,
Buchanan, C. R.
Published in
Journal of inherited metabolic disease
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Journal Of Inherited Metabolic Disease
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Abnormalities, Multiple - Diagnosis
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Biochemistry
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Glucosephosphate Dehydrogenase Deficiency - Complications
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Liver Failure, Acute - Complications
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Liver. Biliary Tract. Portal Circulation. Exocrine Pancreas
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