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Inheritance of the enzyme deficiency in three neurolipidoses: variant 0 of Tay-Sachs disease (Sandhoff's disease), classic tay-sachs disease, and metachromatic leukodystrophy. Identification of the heterozygous carriers

K. Harzer

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Key concepts: Metachromatic leukodystrophy, Sandhoff disease, Tay-Sachs disease, Biology, Hexosaminidase, Arylsulfatase A, Lysosomal storage disease, Krabbe disease

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Inheritance of the enzyme deficiency in three neurolipidoses: variant 0 of Tay-Sachs disease (Sandhoff's disease), classic tay-sachs disease, and metachromatic leukodystrophy. Identification of the heterozygous carriers — Research Paper | ScholarLens