Skip to main content
. 2022 Sep 23;261(3):879–889. doi: 10.1007/s00417-022-05830-3

Fig. 2.

Fig. 2

Pedigrees of CFEOM1 families identified with KIF21A mutations. A-L Genogram and haplotype of CFEOM1 family 01 to 12. Squares represent males, circles represent females, arrows indicate probands, and black symbols identify clinically affected individuals. Eight families (02, 03, 04, 05, 06, 07, 08, and 09) with c.2860C > T (p.R954W), two families (01 and 12) with c.2861G > T (p.R954L), and two families (10 and 11) with c.2861G > A (p.R954Q) were identified. The palpebral fissure length