Gaelle M. Lefevre
Paris, 75012, France
Last Updated: 09/26/2026
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Found 8 publications
Mannose-coupled AAV2: A second-generation AAV vector for increased retinal gene therapy efficiency.
Journal: Molecular therapy. Methods & clinical development
Published: December 14, 2022
Intravitreal air tamponade after AAV2 subretinal injection modifies retinal EGFP distribution.
Journal: Molecular therapy. Methods & clinical development
Published: November 03, 2022
Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: November 24, 2020
A fibered laser system for the MIGA large scale atom interferometer.
Journal: Scientific reports
Published: November 27, 2019
Exploring gravity with the MIGA large scale atom interferometer.
Journal: Scientific reports
Published: May 25, 2018
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.
Journal: European journal of human genetics : EJHG
Published: February 16, 2016
EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss.
Journal: Orphanet journal of rare diseases
Published: April 28, 2015
Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing.
Journal: Molecular genetics & genomic medicine
Published: October 19, 2014
Showing 1-8 of 8
Last Updated: 09/26/2026