Swipe the table sideways for more columns.

TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Genotype/Phenotype Correlation of MORC2 MutationsCharcot-Marie-Tooth disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, central nervous system malformation, developmental disability, hereditary disease, hereditary motor and sensory neuropathy, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, neurodevelopmental disorder, neuromuscular disease, peripheral nervous system disorder, polyneuropathy, psychiatric disorderRecruitingNot stated2026-06-18NCT07038239

1 results · Page 1 of 1

Swipe the table sideways for more columns.

OrganizationsLinked trials
Hospices Civils de Lyon429

12 results · Page 1 of 1

Swipe the table sideways for more columns.

Research sitesCityCountryLinked trials
CH de VersaillesLe ChesnayFrance2
CH Pitié SalpêtrièreParisFrance1
CHRU BrestBrestFrance12
CHU de BesançonBesançonFrance14
CHU de NantesNantesFrance27
CHU de Saint-EtienneSaint-EtienneFrance2
CHU GrenobleGrenobleFrance12
CHU MarseilleMarseilleFrance2
CHU StrasbourgStrasbourgFrance9
Hospices Civils de LyonLyonFrance1
Hôpital NeckerParisFrance13
Service de Génétique moléculaire, pharmacogénétique, hormologie Hôpital BicêtreLe Kremlin-BicêtreFrance1