Neonatal intrahepatic cholestasis associated with citrin deficiency (NICCD): a case series of 11 Malaysian patients
Citrin deficiency, aetiologically linked to mutations of SLC25A13 gene, has two clinical phenotypes, namely adult-onset type II citrullinaemia (CTLN2) and neonatal/infantile intrahepatic cholestasis, caused by citrin deficiency (NICCD). Malaysian patients with NICCD, especially of Malay and East Mal...
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| Main Authors: | , , , , , , |
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| Format: | Article |
| Published: |
Kluwer (now part of Springer)
2010
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| Subjects: | |
| Online Access: | http://eprints.um.edu.my/11879/ |
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