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

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

Bibliographic Details
Main Authors: Yentl Huybrechts, Ellen Steenackers, Neveen Hamdy, Geert Mortier, Guillermo Martinez, Milagros Sierra Bracamonte, Natasha Appelman-Dijkstra, Wim Van Hul, Eveline Boudin
Format: Article
Language:English
Published: Elsevier 2020-10-01
Series:Bone Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2352187220303648

Internet

http://www.sciencedirect.com/science/article/pii/S2352187220303648

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