| Document Date: 2011-01-16 02:52:28
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City Maestri / New York / Portland / / Company Pauli S Linnebank / Tsui LC / McGraw-Hill / Zamora SA / CVS / Suzuki / / Country Japan / / Facility Arch Dis Child / / IndustryTerm mitochondrial aspartate glutamate carrier / aspartate glutamate carrier / Serial diffusion-weighted magnetic resonance imaging / putative mitochondrial carrier protein / / MedicalCondition tremors / neonatal intrahepatic cholestasis / II citrullinemia and idiopathic neonatal hepatitis / JE / Kameya K. Adult-type citrullinemia / Digestive Disease / urea cycle disorders / severe hepatic dysfunction / liver failure / enuresis / hallucinations / coma / Yamano T. Neonatal intrahepatic cholestasis / classical and mild citrullinemia / urea cycle enzyme disorders / CITRULLINEMIA / Elpeleg O. Infantile citrullinemia / intrahepatic cholestasis / Nakano T. Hepatocellular carcinoma / citrin deficiency / idiopathic neonatal hepatitis / deficiency Metabolic Brain Disease / disorder / diarrhea / metabolic disorders / MS / CAUSED BY CITRIN DEFICIENCY / Liver disease / classical citrullinemia / argininosuccinic acid synthetase deficiency / adult-type citrullinemia / ornithine carbamoyltransferase deficiency / insomnia / Hepatocellular carcinoma / Sunohara N. Citrullinemia / Mediterranean citrullinemia / recurrent vomiting / cerebral edema / citrullinemia using citrulline/ornithine / hyperlipidemia / lethargy / II citrullinemia using / Inherited Disease / Pancreatitis / adult-onset citrullinemia / fatty liver / deficiency / CHOLESTASIS / / MedicalTreatment liver transplant / gene therapy / hemodialysis / / Person Sara Copeland / Judith Tuerck / Lee JR / Lorinda Paradise / / Position Walker / / ProgrammingLanguage K / J / / ProvinceOrState Nebraska / New York / / PublishedMedium Natural History / Nature Genetics / The EMBO Journal / / RadioStation Das AM / Lasorsa FM / / Region Mediterranean / / Technology transplantation / MRI / gene therapy / magnetic resonance imaging / spectroscopy / genotype / / URL www.geneclinics.org / /
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Disease Name: CITRULLINEMIA, TYPE 2 (CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2; CITRULLINEMIA, TYPE II, NEONATAL-ONSET; CHOLESTASIS, NEONATAL INTRAHEPATIC, CAUSED BY CITRIN DEFICIENCY)