Identification of the first deletion in the LRP5 gene in a patient with Autosomal Dominant Osteopetrosis type I

Identification of the first deletion in the LRP5 gene in a patient with Autosomal Dominant Osteopetrosis type I

In the last decade, the low-density lipoprotein receptor-related protein 5 (LRP5) gene, coding for a coreceptor in the canonical Wnt signalling pathway, has been shown to play an important role in regulating bone mass and to be involved in the pathogenesis of several bone disorders. Here we describe...

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Bibliographic Details
Main Authors: Pangrazio, Alessandra, Boudin, Eveline, Piters, Elke, Damante, Giuseppe, Iacono, Nadia Lo, D'Elia, Angela Valentina, Vezzoni, Paolo, Van Hul, Wim, Villa, Anna, Sobacchi, Cristina
Format: Online
Language:English
Published: Elsevier Science 2011
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149657/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149657/

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