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

Harzer, K.

Humangenetik 20(1): 9-24

1973


ISSN/ISBN: 0018-7348
PMID: 4776531
DOI: 10.1007/bf00280871
Accession: 043408958

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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