Detection of Tay-Sachs disease heterozygotes by assay of hexosaminidase A in serum and leukocytes
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference14 articles.
1. Tay-Sachs disease: Generalized absence of a beta-N-acetylhexosaminidase component;Okada;Science,1969
2. Variation of β-N-acetylhexosaminidase pattern in Tay-Sachs disease;Sandhoff;FEBS Letters,1969
3. N-Acetylhexosaminidase activities in Tay-Sachs disease;Hultberg;Lancet,1969
4. Demonstration of an alteration of ganglioside metabolism in Tay-Sachs disease;Kolodny;Biochem. Biophys. Res. Comm.,1969
5. Partial deficiency of hexosaminidase component A in juvenile GM2-gangliosidosis;Suzuki;Neurology,1970
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1. Population-based Tay-Sachs screening among Ashkenazi Jewish young adults in the 21st century: Hexosaminidase a enzyme assay is essential for accurate testing;American Journal of Medical Genetics Part A;2009-11
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