Publication | Closed Access

Lysosomal storage disease in the brain: mutations of the β-mannosidase gene identified in autosomal dominant nystagmus

Mendelian DisorderGenetic DisorderGeneticsβ-Mannosidase GeneDegenerative DiseaseNeuroscienceNeurologyNeuropathologyMedicineAutosomal Dominant NystagmusLysosomal Storage DiseaseNeurogenetics