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Huybrechts Y, Boudin E, Hendrickx G, Steenackers E, Hamdy N, Mortier G, Martínez Díaz-Guerra G, Bracamonte MS, Appelman-Dijkstra NM, Van Hul W. Identification of Compound Heterozygous Variants in LRP4 Demonstrates That a Pathogenic Variant outside the Third β-Propeller Domain Can Cause Sclerosteosis. Genes. 2022; 13(1):80. https://doi.org/10.3390/genes13010080

Huybrechts, Yentl, Eveline Boudin, Gretl Hendrickx, Ellen Steenackers, Neveen Hamdy, Geert Mortier, Guillermo Martínez Díaz-Guerra, Milagros Sierra Bracamonte, Natasha M. Appelman-Dijkstra, and Wim Van Hul. 2022. "Identification of Compound Heterozygous Variants in LRP4 Demonstrates That a Pathogenic Variant outside the Third β-Propeller Domain Can Cause Sclerosteosis" Genes 13, no. 1: 80. https://doi.org/10.3390/genes13010080

Huybrechts, Y., Boudin, E., Hendrickx, G., Steenackers, E., Hamdy, N., Mortier, G., Martínez Díaz-Guerra, G., Bracamonte, M. S., Appelman-Dijkstra, N. M., & Van Hul, W. (2022). Identification of Compound Heterozygous Variants in LRP4 Demonstrates That a Pathogenic Variant outside the Third β-Propeller Domain Can Cause Sclerosteosis. Genes, 13(1), 80. https://doi.org/10.3390/genes13010080