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Article

Three novel beta-hexosaminidase A mutations in obligate carriers of Tay-Sachs disease.

Human mutation - 1 Jan 1994

Tomczak J, Grebner E E

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 7951261
DOI: 10.1002/humu.1380040112

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Related research

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Three novel beta-hexosaminidase A mutations in obligate carriers of Tay-Sachs disease.PMID 7951261Read ↗

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Novel mutations, including the second most common in Japan, in the beta-hexosaminidase alpha subunit gene, and a simple screening of Japanese patients with Tay-Sachs disease.Semantic proximity Read ↗

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