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Publications by Francesco Muntoni

A Homozygous COL6A2 Intron Mutation Causes In-Frame Triple-Helical Deletion and Nonsense-Mediated mRNA Decay in a Patient With Ullrich Congenital Muscular Dystrophy

Human Genetics
Genetics
2005English

Steroids in Duchenne Muscular Dystrophy: From Clinical Trials to Genomic Research

Neuromuscular Disorders
Child HealthNeurologyPediatricsPerinatologyGenetics
2002English

Functional Effects of Mutations Identified in Patients With Multiminicore Disease

IUBMB Life
BiochemistryGeneticsClinical BiochemistryCell BiologyMolecular Biology
2007English

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