Author:
Watanabe Yoriko,Numakura Chikahiko,Tahara Toshiyuki,Fukui Kaori,Torimura Takuji,Hiromatsu Yuji,Tomotsune Ken,Yamakawa Mitsunori,Hayasaka Kiyoshi
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine
Reference19 articles.
1. The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein;Kobayashi;Nat Genet,1999
2. Saheki T, Song YZ. Citrin deficiency. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, editors. GeneReviews® [Internet], Seattle: University of Washington; 1993-2019. https://www.ncbi.nlm.nih.gov/books/NBK1181/
3. Steatogenesis in adult- onset type II citrullinemia is associated with down-regulation of PPARα;Komatsu;Biochim Biophys Acta,2015
4. Hayasaka K, Numakura C, Toyota K, Kimura T. Treatment with lactose (galactose)-restricted and medium-chain triglyceride-supplemented formula for neonatal intrahepatic cholestasis caused by citrin deficiency. JIMD Rep 2012;2:37-4. https://doi.org/10.1007/8904_2011_42.
5. Medium-chain triglyceride supplementation under a low-carbohydrate formula is a promising therapy for adult-onset type II citrullinemia;Hayasaka;Mol Genet Metab Rep,2014
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