Z. Zhan

发表

SPG46 and SPG56 are rare causes of hereditary spastic paraplegia in China

B. Tang, Juan Du, Lu Shen, 2016, Journal of Neurology.

A diagnostic gene chip for hereditary spastic paraplegias

K. Xia, Zhengmao Hu, B. Tang, 2013, Brain Research Bulletin.

Association study between SNP rs150689919 in the DNA demethylation gene, TET1, and Parkinson’s disease in Chinese Han population

K. Xia, B. Tang, Ji-feng Guo, 2013, BMC Neurology.

Mutation and Clinical Characteristics of Autosomal-Dominant Hereditary Spastic Paraplegias in China

K. Xia, Q. Pan, B. Tang, 2014, Neurodegenerative Diseases.

SPG35 contributes to the second common subtype of AR‐HSP in China: frequency analysis and functional characterization of FA2H gene mutations

K. Xia, Q. Pan, X. Yan, 2015, Clinical genetics.

Exome sequencing released a case of X-linked adrenoleukodystrophy mimicking recessive hereditary spastic paraplegia.

K. Xia, B. Tang, Xinxiang Yan, 2013, European journal of medical genetics.

Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1

K. Xia, B. Tang, Hong Jiang, 2011, Clinical Neurology and Neurosurgery.

Mutation and Clinical Characteristics of Autosomal-Dominant Hereditary Spastic Paraplegias in China

K. Xia, Q. Pan, B. Tang, 2014, Neurodegenerative Diseases.