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. 2016 Jul 27;11(7):e0160016. doi: 10.1371/journal.pone.0160016

Fig 4. Family 4 from Pakistan with ARS and congenital glaucoma due to a homozygous FOXC1 mutation.

Fig 4

(a) Pedigree and segregation of a novel deletion (c.92_100del; p.Ala31_Ala33del) in the FOXC1 gene. (b). DNA sequence chromatogram of FOXC1 demonstrating loss of codons Ala31-33.