Publication | Closed Access

Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families – Detection of carrier status in symptomatic and asymptomatic female relatives

Rare DiseasesMendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyCarrier StatusPathologyDegenerative DiseaseDystrophin Gene AnalysisDisease Gene IdentificationMedicineAsymptomatic Female RelativesClinical Genetics