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. 2022 Nov 18;101(46):e31872. doi: 10.1097/MD.0000000000031872

Figure 2.

Figure 2.

Identification of ARHGAP4 and CFAP47 mutations in a PHA patient. A-C) A portion of the ARHGAP4 sequence from (A) the patient’s father, (B) the patient’s mother, and (C) the patient, with red frame being used to mark the mutation that was present in the patient but absent in both parents. (D–F) A portion of the CFAP47 sequence from (D) the patient’s father, (E) the patient’s mother, and (F) the patient, with red frame being used to mark the mutation that was present in the patient but absent in both parents.