Associated Papers
Novel variants in the LRP4 underlying Cenani-Lenz Syndactyly syndrome.
Khan H et al.
Journal of Human Genetics, 2022
Deficiency of lrp4 in zebrafish and human LRP4 mutation induce aberrant activation of Jagged-Notch signaling in fin and limb development.
Tian J et al.
Cellular and Molecular Life Sciences : Cmls, 2019
Mutations in the fourth β-propeller domain of LRP4 are associated with isolated syndactyly with fusion of the third and fourth fingers.
Sukenik Halevy R et al.
Human Mutation, 2018
Severe Cenani-Lenz syndrome caused by loss of LRP4 function.
Kariminejad A et al.
American Journal of Medical Genetics. Part A, 2013
LRP4 mutations alter Wnt/beta-catenin signaling and cause limb and kidney malformations in Cenani-Lenz syndrome.
Li Y et al.
American Journal of Human Genetics, 2010
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