Marie-Lucile Figueres

Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations

Graciana Jaureguiberry, Muriel de La Dure‐Molla, David Parry et al. · Nephron Physiology · 2013 · 103 citations · Full text

Medicine, Genetics, Nephrology +16

Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome

S. Hadj‐Rabia, Gaëlle Brideau, Yasser Al‐Sarraj et al. · Genetics in Medicine · 2017 · 103 citations · Full text

Life Sciences, Genetics, Molecular Genetics +4

Claudin-16 Deficiency Impairs Tight Junction Function in Ameloblasts, Leading to Abnormal Enamel Formation

Claire Bardet, Frédéric Courson, Mayssam Khaddam et al. · Journal of Bone and Mineral Research · 2015 · 61 citations

Dentistry, Oral Biology, Pathobiology +17