Yong Gao

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 compound heterozygous mutations in GNPTG in three siblings of a Chinese family with mucolipidosis type III gamma.

Mugen Liu, Q. Wang, Ming-xiong Yuan, 2011, Molecular genetics and metabolism.

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.

FRMD7 Mutations Disrupt the Interaction with GABRA2 and May Result in Infantile Nystagmus Syndrome

P. Yi, Jiuxiang Wang, Lejin Wang, 2020, Investigative ophthalmology & visual science.