Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency in Korean Infants

Citrin is a liver-type mitochondrial aspartate-glutamate carrier encoded by the SLC25A13 gene, and its deficiency causes adult-onset type II citrullinemia and neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD). Here, the authors investigated clinical findings in Korean infants wit...

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Bibliografiset tiedot
Päätekijät: Ko, Jae Sung, Song, Jung Han, Park, Sung Sup, Seo, Jeong Kee
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The Korean Academy of Medical Sciences 2007
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Original Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2694627/
https://ncbi.nlm.nih.gov/pubmed/18162705
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3346/jkms.2007.22.6.952
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