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Investigation of the role of SMN1 and SMN2 haploinsufficiency as a risk factor for Hirayama's disease: Clinical, neurophysiological and genetic characteristics in a Spanish series of 13 patients

Disease SusceptibilityRare DiseasesSmn2 HaploinsufficiencyGenetic DisorderGenetic EpidemiologyPathologyGenetic FactorNeurologyNeuropathologyMedicineGenetic CharacteristicsSpanish Series