Christel Castro
Marseille, 13005, France
Last Updated: 09/26/2026
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Found 12 publications
Benchmarking long-read sequencing approaches to resolve facioscapulohumeral dystrophy locus complexity.
Journal: Brain : a journal of neurology
Published: August 12, 2025
Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot-Marie-Tooth disease 4H.
Journal: Brain : a journal of neurology
Published: March 25, 2022
Clinical and Molecular Update on the Fourth Reported Family with Hamamy Syndrome.
Journal: Molecular syndromology
Published: February 05, 2021
SOX11-related syndrome: report on a new case and review.
Journal: Clinical dysmorphology
Published: October 21, 2020
Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1.
Journal: Human molecular genetics
Published: February 13, 2019
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease.
Journal: Human mutation
Published: May 14, 2015
In-plane organization of silicon nanocrystals embedded in SiO2 thin films.
Journal: Nanotechnology
Published: January 30, 2013
A novel mutation in FGD4/FRABIN causes Charcot Marie Tooth disease type 4H in patients from a consanguineous Tunisian family.
Journal: Annals of human genetics
Published: August 14, 2012
Two novel missense mutations in FGD4/FRABIN cause Charcot-Marie-Tooth type 4H (CMT4H).
Journal: Journal of the peripheral nervous system : JPNS
Published: June 28, 2012
Extraction of the characteristics of Si nanocrystals by the charge pumping technique.
Journal: Nanotechnology
Published: February 02, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026