A Novel Mutation of FOXC1 (R127L) in an Axenfeld-Rieger Syndrome Family with Glaucoma and Multiple Congenital Heart Diseases

Release time:2017-03-30

Impact Factor:1.308

Journal:Ophthalmic Genet

Co-author:Xiang R, Xia K, Li X P, Fan L L, Huang H, Du RF

Indexed by:Unit Twenty Basic Research

Discipline:生物学

Document Type:J

Volume:37

Issue:1

Page Number:111-115

Translation or Not:no

Date of Publication:2016-01-01

Included Journals:SCI

Links to published journals:http://www.tandfonline.com/doi/full/10.3109/13816810.2014.924016