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Diagram showing five groups with different types of FOXL2 mutations. Groups A to C: truncated proteins, with partial forkhead domain (Group A), with complete forkhead and without complete polyalanine tract (Group B), and with complete forkhead and polyalanine domain (Group C). Group D: duplication mutations leading to elongated polyalanine tract, group E: missense and single amino acid insertion mutations in forkhead domain.
