Benjamin Navet
Angers, France
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 12 publications
Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.
Journal: American journal of human genetics
Published: February 06, 2026
Bi-allelic variants in DOHH, catalyzing the last step of hypusine biosynthesis, are associated with a neurodevelopmental disorder.
Journal: American journal of human genetics
Published: November 09, 2021
De novo missense variants in LMBRD2 are associated with developmental and motor delays, brain structure abnormalities and dysmorphic features.
Journal: Journal of medical genetics
Published: April 24, 2020
Contribution of the SYK Tyrosine kinase expression to human iNKT self-reactivity.
Journal: European journal of immunology
Published: September 23, 2019
Maternal RANKL Reduces the Osteopetrotic Phenotype of Null Mutant Mouse Pups.
Journal: Journal of clinical medicine
Published: October 12, 2018
Bone resorption: an actor of dental and periodontal development?
Journal: Frontiers in physiology
Published: July 31, 2015
Skeletal consequences of RANKL-blocking antibody (IK22-5) injections during growth: mouse strain disparities and synergic effect with zoledronic acid.
Journal: Bone
Published: September 02, 2014
Showing 1-12 of 12
Last Updated: 09/26/2026