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The Lrp4R1170Q homozygous knock-in mouse recapitulates the bone phenotype of sclerosteosis in humans
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Genetic control of bone mass
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Further delineation of facioaudiosymphalangism syndrome : description of a family with a novel NOG mutation and without hearing loss
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Eight mutations including 5 novel ones in the COL1A1 gene in Czech patients with osteogenesis imperfecta
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A novel domain-specific mutation in a sclerosteosis patient suggests a role of LRP4 as an anchor for sclerostin in human bone
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- Journal Article
- A1
- open access
Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta
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Sclerosing bone dysplasias : leads toward novel osteoporosis treatments
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Variation in the Kozak sequence of WNT16 results in an increased translation and is associated with osteoporosis related parameters
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The role of extracellular modulators of canonical Wnt signaling in bone metabolism and diseases
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Mutations in sFRP1 or sFRP4 are not a common cause of craniotubular hyperostosis