Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity

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Korvala , J , Jueppner , H , Mäkitie , O , Sochett , E , Schnabel , D , Mora , S , Bartels , C F , Warman , M L , Deraska , D , Cole , W G , Hartikka , H , Ala-Kokko , L & Mannikko , M 2012 , ' Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity ' , BMC Medical Genetics , vol. 13 , 26 . https://doi.org/10.1186/1471-2350-13-26

Title: Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity
Author: Korvala, Johanna; Jueppner, Harald; Mäkitie, Outi; Sochett, Etienne; Schnabel, Dirk; Mora, Stefano; Bartels, Cynthia F.; Warman, Matthew L.; Deraska, Donald; Cole, William G.; Hartikka, Heini; Ala-Kokko, Leena; Mannikko, Minna
Contributor organization: Lastentautien yksikkö
Children's Hospital
HUS Children and Adolescents
Date: 2012
Language: eng
Number of pages: 10
Belongs to series: BMC Medical Genetics
ISSN: 1471-2350
DOI: https://doi.org/10.1186/1471-2350-13-26
URI: http://hdl.handle.net/10138/164116
Subject: IDIOPATHIC JUVENILE OSTEOPOROSIS
RECEPTOR-RELATED PROTEIN-5
BONE-MASS
PSEUDOGLIOMA SYNDROME
MISSENSE MUTATIONS
GENE-EXPRESSION
MULTIPLE-MYELOMA
DENSITY
INHIBITION
BINDING
3123 Gynaecology and paediatrics
Peer reviewed: Yes
Rights: cc_by
Usage restriction: openAccess
Self-archived version: publishedVersion


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