Katherine Mathews

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Clinical Trial Readiness for the Dystroglycanopathies	Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Malformations of Cortical Development, Group II, Muscular Disorders, Atrophic, autosomal recessive limb-girdle muscular dystrophy type 2I, autosomal recessive limb-girdle muscular dystrophy type 2M, central nervous system malformation, cerebral cortical dysplasia, cobblestone lissencephaly, eye disorder, hereditary disease, lissencephaly spectrum disorders, muscle tissue disorder, muscular dystrophy, muscular dystrophy-dystroglycanopathy, type A, musculoskeletal system disorder, nervous system disorder, neuromuscular disease	Recruiting	Not stated	2025-07-30		NCT00313677

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