J. Chen

[Association between rare UBQLN2 variants and amyotrophic lateral sclerosis in Chinese population].

D. Fan, J. Chen, X. Y. Liu, 2021, Zhonghua yi xue za zhi.

A novel PNPLA2 mutation causes neutral lipid storage disease with myopathy (NLSDM) presenting muscular dystrophic features with lipid storage and rimmed vacuoles.

Y. Yuan, D. Hong, Z. Wang, 2010, Clinical neuropathology.

[Harlequin fetus--a case report].

W. Hsu, J. Chen, C. Tsay, 1989, Zhonghua yi xue za zhi = Chinese medical journal; Free China ed.

[Pathogenic gene variants and clinical phenotype features of 26 children with progressive myoclonic epilepsy].

T. Ji, L. P. Zhang, W. Sun, 2019, Zhonghua er ke za zhi = Chinese journal of pediatrics.

[Genotype-phenotype correlation in patients with alternating hemiplegia of childhood].

Q. Zeng, X. Wu, J. Chen, 2018, Zhonghua er ke za zhi = Chinese journal of pediatrics.

Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese

M. Farrer, A. Singleton, J. Hardy, 2000, Neurology.

[Clinical features of epilepsies associated with GABRB2 variants].

X. Wu, J. Chen, X. Yang, 2019, Zhonghua er ke za zhi = Chinese journal of pediatrics.