Missense variants in homeobox domain of PBX1 cause coracoclavicular ankylosis

  • Mary L, Leclerc D, Gilot D, Belaud-Rotureau MA, Jaillard S. The TALE never ends: A comprehensive overview of the role of PBX1, a TALE transcription factor, in human developmental defects. Hum Mutat. 2022;43:1125–48.

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