Spanish Natural History Study for LAMA2 Muscular Dystrophy | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Spanish Natural History Study for LAMA2 Muscular Dystrophy	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, Muscular dystrophy congenital, merosin negative, hereditary disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular disease	Recruiting	Not stated	2025-04-11		NCT06924125

2 results · Page 1 of 1

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Organizations	Linked trials
ASOCIACIÓN IMPÚLSATE PARA LA CURA DE LOS NIÑOS CON DÉFICIT DE MEROSINA	1
Hospital Universitari Vall d'Hebron Research Institute	64

1 results · Page 1 of 1

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Research sites	City	Country	Linked trials
University Hospital Vall d'Hebron	Barcelona	Spain	1