Xiaorong Hou

发表

The Clinical and Polynucleotide Repeat Expansion Analysis of ATXN2, NOP56, AR and C9orf72 in Patients With ALS From Mainland China

B. Tang, Junling Wang, Zhen Liu, 2022, Frontiers in Neurology.

Identification of GGC repeat expansion in the NOTCH2NLC gene in amyotrophic lateral sclerosis

B. Tang, Hong Jiang, Lu Shen, 2020, Neurology.

Association of variants in the KIF1A gene with amyotrophic lateral sclerosis

B. Tang, Ji-feng Guo, Zhuohua Zhang, 2022, Translational Neurodegeneration.

Gene4MND: An Integrative Genetic Database and Analytic Platform for Motor Neuron Disease

Guihu Zhao, Jinchen Li, B. Tang, 2021, Frontiers in Molecular Neuroscience.

Mutation spectrum of amyotrophic lateral sclerosis in Central South China

B. Tang, Ling Huang, Hong Jiang, 2021, Neurobiology of Aging.

A Novel Potentially Pathogenic Rare Variant in the DNAJC7 Gene Identified in Amyotrophic Lateral Sclerosis Patients From Mainland China

B. Tang, Ling Huang, Hong Jiang, 2020, Frontiers in Genetics.

ALS-plus related clinical and genetic study from China

Qianchuan Zhao, B. Tang, Ji-feng Guo, 2023, Neurological Sciences.

Rare, pathogenic variants in LRP10 are associated with amyotrophic lateral sclerosis in patients from mainland China

Jinchen Li, B. Tang, Ling Huang, 2020, Neurobiology of Aging.

Mitochondrial genome variations are associated with amyotrophic lateral sclerosis in patients from mainland China

Mingyu Liang, B. Tang, Hong Jiang, 2021, Journal of Neurology.