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
- 1 January 1973
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 20 (1) , 9-24
- https://doi.org/10.1007/bf00280871
Abstract
No abstract availableKeywords
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