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DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy

Rare DiseasesMendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyMolecular BiologyDegenerative DiseaseMolecular GeneticsDisease Gene IdentificationFounder EffectMedicineNorth American FamiliesClinical Genetics