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Screening of nine SLC25A13 mutations: their frequency in patients with citrin deficiency and high carrier rates in Asian populations.
Mol Genet Metab. 2003 Nov;80(3):356-9. doi: 10.1016/S1096-7192(03)00140-9.
Mol Genet Metab. 2003.
PMID: 14680984
Pathogenesis of adult-onset type II citrullinemia caused by deficiency of citrin, a mitochondrial solute carrier protein: tissue and subcellular localization of citrin.
Iijima M, Jalil A, Begum L, Yasuda T, Yamaguchi N, Xian Li M, Kawada N, Endou H, Kobayashi K, Saheki T.
Iijima M, et al. Among authors: xian li m.
Adv Enzyme Regul. 2001;41:325-42. doi: 10.1016/s0065-2571(00)00022-4.
Adv Enzyme Regul. 2001.
PMID: 11384753
No abstract available.
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