ALX4

(redirected from PFM2)

ALX4

A gene on chromosome 11p11.2 that encodes a homeodomain transcription factor, which may play a role in craniofacial development, mesenchymal-epithelial communication and hair-follicle development.

Molecular pathology
ALX4 mutations cause parietal foramina 2 and Potocki-Shaffer syndrome.
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702** better decisions by the project team (a) PFM2 The supplier's involvement in this project led to 0.