Acute liver failure with subsequent cirrhosis as the primary manifestation of TRMU mutations
- Author
- SCHARA, Ulrike1 ; VON KLEIST-RETZOW, Jürgen-Christoph2 3 ; HORVATH, Rita5 7 ; LAINKA, Elke4 ; GERNER, Patrick4 ; PYLE, Angela5 6 ; SMITH, Paul M5 ; LOCHMÜLLER, Hanns6 ; CZERMIN, Birgit7 ; ABICHT, Angela7 ; HOLINSKI-FEDER, Elke7
[1] Pediatric Neurology, University of Essen, Essen, Germany
[2] Department of Pediatrics, University of Cologne, Cologne, Germany
[3] Center for Molecular Medicine CMMC, University of Cologne, Cologne, Germany
[4] Pediatric Gastroenterology, University of Essen, Essen, Germany
[5] Mitochondrial Research Group, Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne, United Kingdom
[6] Institute of Human Genetics, Newcastle University, Central Parkway, Newcastle upon Tyne NE1 3BZ, United Kingdom
[7] Medical Genetics Center, Munich, Germany - Source
Journal of inherited metabolic disease. 2011, Vol 34, Num 1, pp 197-201, 5 p ; ref : 3/4 p
- CODEN
- JIMDDP
- ISSN
- 0141-8955
- Scientific domain
- Genetics; Nutrition, obesity, metabolic disorders
- Publisher
- Springer, Heidelberg
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aigu Cirrhose Evolution Génétique Insuffisance hépatique Maladie héréditaire Maladie métabolique Mutation Nutrition Primaire Pathologie de l'appareil digestif Pathologie du foie
- Keyword (en)
- Acute Cirrhosis Evolution Genetics Liver failure Genetic disease Metabolic diseases Mutation Nutrition Primary Digestive diseases Hepatic disease
- Keyword (es)
- Agudo Cirrosis Evolución Genética Insuficiencia hepática Enfermedad hereditaria Metabolismo patología Mutación Nutrición Primario Aparato digestivo patología Hígado patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B13 Gastroenterology. Liver. Pancreas. Abdomen / 002B13C Liver. Biliary tract. Portal circulation. Exocrine pancreas / 002B13C03 Other diseases. Semiology
- Discipline
- Gastroenterology. Liver. Pancreas. Abdomen Medical genetics Metabolic diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 23861874
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1007/s10545-010-9250-z 
https://dx.doi.org/10.1007/s10545-010-9250-z
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