Assignment of the human gene for hexosaminidase B to chromosome 5
Author:
Publisher
Elsevier BV
Subject
Cell Biology
Reference12 articles.
1. Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase Component
2. Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs
3. Genetic complementation after fusion of Tay-Sachs and Sandhoff cells
4. Tay-Sachs and Sandhoff's disease: Intergenic complementation after somatic cell hybridization
5. Assignment of a Locus Involved in the Expression of Hexosaminidase A to Chromosome 7 in Man
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