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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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| Главные авторы: | , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
The Korean Academy of Medical Sciences
2007
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| Предметы: | |
| Online-ссылка: | 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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