X. Dai

Identification and functional characterization of a novel splicing mutation in RP gene PRPF31.

Mugen Liu, X. Tu, Xu Wang, 2008, Biochemical and biophysical research communications.

Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis

Mugen Liu, M. Sobrido, Haibo Xu, 2012, Nature Genetics.

Identification of a novel genetic locus on chromosome 8p21.1–q11.23 for idiopathic basal ganglia calcification

Mugen Liu, Haibo Xu, Q. Wang, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation

Mugen Liu, Q. Wang, X. Ren, 2007, Journal of Human Genetics.

Molecular genetic analysis of partial 9p trisomy in two Chinese families with mental retardation and facial anomaly

Ai-ping Feng, N. Zhang, Jingyu Liu, 2011, Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban.

[Cytogenetic analysis of partial trisomy 9p resulting from a reciprocal balanced 9/21 translocation].

Jing-Yu Liu, X. Dai, Xiao-Ran Wang, 2007, Yi chuan = Hereditas.

[Two variants in MYOC and CYP1B1 genes in a Chinese family with primary angle-closure glaucoma].

Qing Wang, Mugen Liu, X. Dai, 2008, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.