The Mutations in Ashkenazi Jews with Adult G M2 Gangliosidosis, the Adult Form of Tay-Sachs Disease-Reference-Cited by-同舟云学术

The Mutations in Ashkenazi Jews with Adult G M2 Gangliosidosis, the Adult Form of Tay-Sachs Disease

Published:1989-03-17 Issue:4897 Volume:243 Page:1471-1474
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Navon Ruth¹,Proia Richard L.¹

Affiliation:

1. Genetics and Biochemistry Branch, National Institute of Diabetes, Digestive, and Kidney Diseases, Bethesda, MD 20892.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference45 articles.

1. ARPAIA, E, IDENTIFICATION OF AN ALTERED SPLICE SITE IN ASHKENAZI TAY-SACHS DISEASE, NATURE 333: 85 (1988).

2. AVIV, H, PURIFICATION OF BIOLOGICALLY-ACTIVE GLOBIN MESSENGER-RNA BY CHROMATOGRAPHY ON OLIGOTHYMIDYLIC-ACID-CELLULOSE, PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 69: 1408 (1972).

3. BAYLERAN, J, SYNTHESIS OF 4-METHYLUMBELLIFERYL-BETA-D-N-ACETYLGLUCOSAMINE-6-SULFATE AND ITS USE IN CLASSIFICATION OF GM2 GANGLIOSIDOSIS GENOTYPES, CLINICA CHIMICA ACTA 143: 73 (1984).

4. CHIRGWIN, J.M., ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE, BIOCHEMISTRY 18: 5294 (1979).

5. CONZELMANN, E, GANGLIOSIDE-GM2 N-ACETYL-BETA-D-GALACTOSAMINIDASE ACTIVITY IN CULTURED FIBROBLASTS OF LATE-INFANTILE AND ADULT GM2-GANGLIOSIDOSIS PATIENTS AND OF HEALTHY PROBANDS WITH LOW HEXOSAMINIDASE LEVEL, AMERICAN JOURNAL OF HUMAN GENETICS 35: 900 (1983).

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