A Case of Adult Onset Type II Citrullinemia with SLC25A13 Gene Mutation
Author:
Affiliation:
1. Division of Endocrinology, Department of Internal Medicine, College of Medicine, Chosun University, Korea.
2. Green Cross Reference Laboratory, Korea.
Publisher
Korean Endocrine Society
Link
https://synapse.koreamed.org/pdf/10.3803/jkes.2006.21.6.542
Reference18 articles.
1. MAMMALIAN UREA CYCLE ENZYMES
2. Hereditary disorders of the urea cycle in man: Biochemical and molecular approaches
3. Pathogenesis of adult-onset type II citrullinemia caused by deficiency of citrin, a mitochondrial solute carrier protein: tissue and subcellular localization of citrin
4. The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein
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