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Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within a single large kindred and map to a refined region on chromosome 7p15

Chromosome 7P15Mendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene IdentificationRefined RegionMedicine