| Document Date: 2007-06-25 16:35:49
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City New York / / Company Zamora SA / Pauli S Linnebank / Suzuki / Tsui LC / McGraw-Hill / / Facility Arch Dis Child / / IndustryTerm aspartate glutamate carrier / magnetic resonance imaging / mitochondrial aspartate glutamate carrier / putative mitochondrial carrier protein / / MedicalCondition adult-type citrullinemia / ornithine carbamoyltransferase deficiency / neonatal intrahepatic cholestasis / JE / Kameya K. Adult-type citrullinemia / Digestive Disease / urea cycle disorders / severe hepatic dysfunction / CLASSIC CITRULLINEMIA / Sunohara N. Citrullinemia / ARGININOSUCCINATE SYNTHETASE DEFICIENCY / Mediterranean citrullinemia / classical and mild citrullinemia / Yamano T. Neonatal intrahepatic cholestasis / urea cycle enzyme disorders / CITRULLINEMIA / citrullinemia using citrulline/ornithine / Elpeleg O. Infantile citrullinemia / II citrullinemia using / Nakano T. Hepatocellular carcinoma / citrin deficiency / Inherited Disease / idiopathic neonatal hepatitis / deficiency Metabolic Brain Disease / ASS DEFICIENCY / adult-onset citrullinemia / deficiency / metabolic disorders / classical citrullinemia / argininosuccinic acid synthetase deficiency / / MedicalTreatment gene therapy / hemodialysis / / Person Lee JR / / Position Walker / / ProgrammingLanguage J / K / / ProvinceOrState New York / / PublishedMedium Nature Genetics / The EMBO Journal / / RadioStation Lasorsa FM / Das AM / / Region Mediterranean / / Technology gene therapy / magnetic resonance imaging / spectroscopy / transplantation / genotype / MRI / / URL www.geneclinics.org / /
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CLASSIC CITRULLINEMIA (ASS) REFERENCES (CITRULLINEMIA, TYPE I; CTLN1; ARGININOSUCCINATE SYNTHETASE DEFICIENCY; ASS DEFICIENCY) 1. 2.