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. 2020 May 23;56:102792. doi: 10.1016/j.ebiom.2020.102792

Fig. 1.

Fig 1

Pedigrees and sequences of the five homozygous loss-of-function variants in ENSA, DACT2, EXTL2, DDR1, and CCDC188. The genotypes of all probands and available family members are shown below each individual. The blackened symbols represent affected individuals. Mx, mutant alleles; +, wild-type allele.