Characterization of a novel FOXC1 mutation, P297S, identified in two individuals with anterior segment dysgenesis

  • Clin Genet. 2009 Sep;76(3):296-9. doi: 10.1111/j.1399-0004.2009.01210.x.
C D Fetterman ,  F Mirzayans ,  M A Walter
PMID: 19793056 DOI: 10.1111/j.1399-0004.2009.01210.x