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Chern T, Achilleos A, Tong X, et al. (2022) Mutations in Hcfc1 and Ronin result in an inborn error of cobalamin metabolism and ribosomopathy. Nature Communications. 13: 134 |
Chern T, Achilleos A, Tong X, et al. (2020) Mouse models to study the pathophysiology of combined methylmalonic acidemia and homocystinuria, cblC type. Developmental Biology |
Chen WC, Wu KC, Hu CH, et al. (2011) A compound heterozygous mutation of CYP27A1 gene in a Taiwanese patient with cerebrotendinous xanthomatosis. Journal of Orthopaedic Science : Official Journal of the Japanese Orthopaedic Association. 16: 825-7 |
Chern TM, Paul N, van Nimwegen E, et al. (2008) Computational analysis of full-length cDNAs reveals frequent coupling between transcriptional and splicing programs. Dna Research : An International Journal For Rapid Publication of Reports On Genes and Genomes. 15: 63-72 |