A novel FBN1 mutation causes autosomal dominant Marfan syndrome

Xiao, Y; Liu, XQ; Guo, XX; Liu, LP; Jiang, LX; Wang, Q; Gong, B

Wang, Q (reprint author), Shandong Univ, Shandong Prov Hosp, Dept Ophthalmol, 324 Jingwu Rd, Jinan 250021, Shandong, Peoples R China.; Gong, B (reprint author), Hosp Univ Elect Sci & Technol China, Sichuan Prov Key Lab Dis Gene Study, 32 Rd West 2,First R

MOLECULAR MEDICINE REPORTS, 2017; 16 (5): 7321

Abstract

Marfan syndrome (MFS) is an inherited and systemic disorder. It has been reported that mutations in the fibrillin-1 gene (FBN1) account for similar to......

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