CHU Marseille

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Genotype/Phenotype Correlation of MORC2 Mutations	Charcot-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 disorder	Recruiting	Not stated	2026-06-18		NCT07038239
Cardiac Amyloidosis pRevaleNce of in OLDer Subjects Affected by Heart Failure	Amyloid Neuropathies, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, amyloidosis, familial amyloid neuropathy, hereditary amyloidosis, hereditary disease, inborn errors of metabolism, inherited neurodegenerative disorder, metabolic disease, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, proteostasis deficiencies	Recruiting	Not stated	2026-04-20		NCT06427304

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