Associated Papers
Genomic Analysis of Korean Patient With Microcephaly.
Lee J et al.
Frontiers in Genetics, 2020
33584783 (PubMed )
Supplement: Table_3.xlsx › Supplementary_Table_3
Early loss of mitochondrial complex I and rewiring of glutathione metabolism in renal oncocytoma.
Gopal RK et al.
Proceedings of the National Academy of Sciences of the United States of America, 2018
29915083 (PubMed )
Supplement: pnas.1711888115.sd01.xlsx › Exome_Variants
Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ-glutamyltransferase cholestasis.
Qiu YL et al.
Hepatology (baltimore, Md.), 2017
28027573 (PubMed )
Supplement: HEP-65-1655-s001.pdf
Variants in the UBR1 gene are not associated with chronic pancreatitis in Japan.
Masamune A et al.
Pancreatology : Official Journal of the International Association of Pancreatology (iap) ... [et Al.], 0
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