WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders

by Yentl Huybrechts, Geert Mortier, Eveline Boudin, Wim Van Hul
Published 2020-04-01

Compound heterozygosity of mutations located in the first and third β-propeller domain of LRP4 causes sclerosteosis in a Spanish patient

by Yentl Huybrechts, Ellen Steenackers, Neveen Hamdy, Geert Mortier, Guillermo Martinez, Milagros Sierra Bracamonte, Natasha Appelman-Dijkstra, Wim Van Hul, Eveline Boudin
Published 2020-10-01