2. Academic Validation
  3. Characterization of a novel FOXC1 mutation, P297S, identified in two individuals with anterior segment dysgenesis

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
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