Publication | Open Access

Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in Taiwan: implications for low prevalence and founder mutations of Taiwanese myotonic dystrophy type 1

Mendelian DisorderGenetic DisorderGeneticsHaplotype AnalysisGenetic EpidemiologyClinical GeneticsPathologyDegenerative DiseaseLow PrevalenceDisease Gene IdentificationPublic HealthMedicineFounder MutationsMonogenic Disorders