A novel sequence variant in SFRP4 causing Pyle disease

Chelna Galada1, Hitesh Shah2, Anju Shukla1

  • 1Department of Medical Genetics, Kasturba Medical College, Manipal University, Manipal, India.

Journal of Human Genetics
|January 20, 2017
PubMed
Summary

Pyle disease (PYL) is a rare bone disorder. A novel mutation in the SFRP4 gene was identified in a patient, confirming its role in PYL development.

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