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Molecular analysis of the dystrophin gene in 407 Chinese patients with Duchenne/Becker muscular dystrophy by the combination of multiplex ligation-dependent probe amplification and Sanger sequencing

Duchenne/becker Muscular DystrophyDystrophin GeneMendelian DisorderGenetic DisorderMedicineGeneticsPathologyDisease Gene IdentificationMolecular DiagnosticsBioinformaticsChinese Patients