Elodie Lebredonchel

4PUBLICATIONS
10CO-AUTHORS
Central and Eastern European languages (incl. Russian)Gene and molecular therapyPsychosocial aspects of childbirth and perinatal mental healthOphthalmology and optometry not elsewhere classified
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Publications (4)

|Oct 11, 2022
A PMM2-CDG caused by an A108V mutation associated with a heterozygous 70 kilobases deletion case report.

E Lebredonchel, A Riquet, D Neut

|Nov 12, 2021
Variation of the serum N-glycosylation during the pregnancy of a MPI-CDG patient.

Elodie Lebredonchel, Sandrine Duvet, Claire Douillard

|Jul 02, 2021
Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy.

Vasily Smirnov, Olivier Grunewald, Jean Muller

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