Associated Papers
Ureteropelvic junction obstruction with primary lymphoedema associated with CELSR1 variants.
Alpaslan M et al.
Journal of Medical Genetics, 2023
Lymphedema complicated by protein-losing enteropathy with a 22q13.3 deletion and the potential role of CELSR1: A case report.
Xia S et al.
Medicine, 2021
Increasing evidence of hereditary lymphedema caused by CELSR1 loss-of-function variants.
Maltese PE et al.
American Journal of Medical Genetics. Part A, 2019
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