Tooze RS, Calpena E, Twigg SRF, D'Arco F, et al. Craniosynostosis, inner ear, and renal anomalies in a child with complete loss of
SPRY1 (sprouty homolog 1) function. J Med Genet 2022 Dec 21:jmg-2022-108946. doi: 10.1136/jmg-2022-108946.
PMID: 36543535