Yang Wang

[Clinical features of infantile neuroaxonal dystrophy and PLA2G6 gene testing].

Chun-Hua Liu, Yao Lu, Yang Wang, 2019, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia

C. Prange, G. Lennon, J. Lawler, 1995, Nature Genetics.

De novo variations of ANK1 gene caused hereditary spherocytosis in two Chinese children by affecting pre-mRNA splicing

Jie Yu, Xizhou An, Yao Zhu, 2023, BMC Pediatrics.

The novel compound heterozygous variants identified in a Chinese family with glucose phosphate isomerase deficiency and pathogenicity analysis

Tao Liu, Y. Xiang, Jiaqi Liu, 2023, BMC Medical Genomics.

Familial partial lipodystrophy with gene mutation in both LMNA and PPARG : report of a case and review of literature

Gui-ming Zhou, Meiqi Xu, Yang Wang, 2016 .