Xuntai Ma

A novel mutation impairing the tertiary structure and stability of γC‐crystallin (CRYGC) leads to cataract formation in humans and zebrafish lens

P. Li, Juhua Yang, Yong-Bin Yan, 2012, Human mutation.

A Novel CRYGD Mutation (p.Trp43Arg) Causing Autosomal Dominant Congenital Cataract in a Chinese Family

Binbin Wang, Jing Wang, Sirui Zhou, 2011, Human mutation.

A missense mutation in the gammaD-crystallin gene CRYGD associated with autosomal dominant congenital cataract in a Chinese family.

Feng Gu, Xu Ma, S. Huang, 2006, Molecular vision.

The roles of two novel FBN1 gene mutations in the genotype-phenotype correlations of Marfan syndrome and ectopia lentis patients with marfanoid habitus.

Feng Gu, Xu Ma, Dan Li, 2008, Genetic testing.

Novel -Crystallin Gene Mutations in Chinese Families With Nuclear Cataracts

Fengju Zhang, Si-quan Zhu, K. Wang, 2011 .

The roles of two novel FBN1 gene mutations in the genotype-phenotype correlations of Marfan syndrome and ectopia lentis patients with marfanoid habitus.

Feng Gu, Dan Li, N. Liu, 2008, Genetic testing.