Associated Papers
Case report: Identification of novel fibrillin-2 variants impacting disulfide bond and causing congenital contractural arachnodactyly.
Li AL et al.
Frontiers in Genetics, 2023
Identification of Novel FBN2 Variants in a Cohort of Congenital Contractural Arachnodactyly.
Sun L et al.
Frontiers in Genetics, 2022
A novel FBN2 mutation in a Chinese family with congenital contractural arachnodactyly.
Liu W et al.
Febs Open Bio, 2015
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