J. Zeng

Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China

K. Xia, Q. Pan, X. Yan, 2016, Clinical genetics.

SCA38 is rare in mainland China

B. Tang, Hong Jiang, Lu Shen, 2015, Journal of the Neurological Sciences.

Spinocerebellar ataxia type 21 exists in the Chinese Han population

K. Xia, Q. Pan, B. Tang, 2016, Scientific Reports.

PRRT2 frameshift mutation reduces its mRNA stability resulting loss of function in paroxysmal kinesigenic dyskinesia.

L. Mei, B. Tang, W. Xiong, 2019, Biochemical and biophysical research communications.

C9ORF72 repeat expansion is not detected in sporadic ataxia patients in mainland China

B. Tang, Hong Jiang, Lu Shen, 2016, Journal of the Neurological Sciences.

Chinese homozygous Machado–Joseph disease (MJD)/SCA3: a case report

B. Tang, Hong Jiang, S. Zeng, 2015, Journal of Human Genetics.

Friedreich's Ataxia (FRDA) is an extremely rare cause of autosomal recessive ataxia in Chinese Han population

B. Tang, Hong Jiang, S. Zeng, 2015, Journal of Neurological Sciences.