Zhiqiang Lin

发表

One PMP22/MPZ and Three MFN2/GDAP1 Concomitant Variants Occurred in a Cohort of 189 Chinese Charcot-Marie-Tooth Families

B. Tang, Ji-feng Guo, Lu Shen, 2022, Frontiers in Neurology.

Genotype and phenotype distribution of 435 patients with Charcot–Marie–Tooth disease from central south China

Zhengmao Hu, B. Tang, S. Zuchner, 2021, European journal of neurology.

Genetic and Clinical Features in 24 Chinese Distal Hereditary Motor Neuropathy Families

Zhengmao Hu, B. Tang, Ji-feng Guo, 2020, Frontiers in Neurology.

Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

Dana M. Bis-Brewer, R. Finkel, F. Muntoni, 2020, Nature Genetics.

SPTLC1 p.Leu38Arg, a novel mutation associated with childhood ALS

T. Hornemann, B. Tang, S. Zeng, 2022, medRxiv.

A novel WARS mutation (p.Asp314Gly) identified in a Chinese distal hereditary motor neuropathy family

Jun Liu, Zhengmao Hu, B. Tang, 2019, Clinical genetics.

The genetic and clinical spectrum in a cohort of 39 families with complex inherited peripheral neuropathies

B. Tang, S. Zuchner, Q. Xiao, 2023, Journal of Neurology.

Clinical and genetic features of Charcot-Marie-Tooth disease patients with IGHMBP2 mutations

B. Tang, L. Lei, Xiao-bo Li, 2022, Neuromuscular Disorders.

Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

Dana M. Bis-Brewer, R. Finkel, F. Muntoni, 2020, Nature Genetics.

Phenotype-driven reanalysis reveals five novel pathogenic variants in 40 exome-negative families with Charcot–Marie–Tooth Disease

Xiao-bo Li, Lei Liu, Yongzhi Xie, 2023, Journal of neurology.

Genotype–phenotype characteristics and baseline natural history of Chinese myelin protein zero gene related neuropathy patients

B. Tang, Xiao-bo Li, Lei Liu, 2023, European journal of neurology.