Ching-Ching Ng

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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a rare hereditary stroke caused by mutations in NOTCH3 gene. We report the first case of CADASIL in an indigenous Rungus (Kadazan-Dusun) family in Kudat, Sabah, Malaysia confirmed by a R54C (c.160C>T, p.Arg54Cys) mutation in the NOTCH3. This mutation was(More)
Large consortia efforts and genome-wide association studies (GWASs) have linked a number of genetic variants within the 6p21 chromosomal region to non-Hodgkin lymphoma (NHL). Complementing these efforts, we genotyped previously reported SNPs in the human leukocyte antigen (HLA) class I (rs6457327) and class II (rs9271100, rs2647012 and rs10484561) regions(More)
The images for figures Figs 2 and 3 are swapped. The image for Fig 2 should be Fig 3 and the image for Fig 3 should be Fig 2. The figure captions are correct. The publisher apologizes for the error. Please see the corrected Figs 2 and 3 here. Fig 2. Electron microscopy of skin biopsy shows electron dense granular deposits (arrows) in the basal lamina(More)
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