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. 2020 May 7;57(6):405–413. doi: 10.1136/jmedgenet-2019-106411

Figure 1.

Figure 1

Pedigrees with multiple rare damaging variants within AIS-associated genes. Filled symbols for men (squares) and women (circles) denote affected individuals, and empty symbols indicate unaffected individuals. Individuals with heterozygous variants are indicated with ‘m/−’, while ‘−/−’ indicates wild type. AIS, adolescent idiopathic scoliosis.