Publications

Dong Y, Wang RM, Yang GM, et al. Role for Biochemical Assays and Kayser-Fleischer Rings in Diagnosis of Wilson's Disease. Clin Gastroenterol Hepatol 2021;19:590-596.

Chen YC, Yu H, Wang RM, Xie JJ, Ni W, Dong Y*,   Wu ZY*. Contribution of intragenic deletions to   mutation spectrum in Chinese patients with Wilson's disease and possible   mechanism underlying ATP7B gross deletions. Parkinsonism & related disorders 2019, 62: 128-133.

Dong Y, Ni   W, Chen WJ, Wan B, Zhao GX, Shi ZQ, Zhang Y, Wang N, Yu L, Xu JF, Wu ZY.   Specturm and classification of ATP7B variants in a large cohort of Chinese patients with Wilson's disease guides genetic diagnosis. Theranostics. 2016;6(5):638-49.

Dong Y, Shi   SS, Chen S, Ni W, Zhu M, Wu ZY. The discrepancy between the absence of copper deposition and the presence of neuronal damage in the brain of Atp7b(-/-) mice. Metallomics : integrated biometal science. 2015;7:283-8.

Dong Y, Wu JJ, Wu ZY. Identification of 46 CAG repeats within   PPP2R2B as probably the shortest pathogenic allele for SCA12. Parkinsonism & related disorders. 2015;21:398-401.

Dong Y, Sun YM, Liu ZJ, Ni W, Shi SS, Wu ZY. Chinese patients with Huntington's disease initially presenting with spinocerebellar ataxia. Clinical genetics. 2013;83:380-3.

Dong Y, Sun YM, Ni W, Gan SR, Wu ZY. Chinese patients with spinocerebellar ataxia type 3 presenting with rare clinical symptoms. Journal of the neurological sciences. 2013;324:167-71.

Dong Y, Sun Y-M, Wu Z-Y. The importance of deep exploration into clinical heterogeneity of spinocerebellar ataxia type 3. Journal of the neurological sciences. 2013;326:122.