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Prenatal diagnosis and carrier detection of genetic diseases by analysis of deoxyribonucleic acid

✍ Scribed by Harry Ostrer; J. Fielding Hejtmancik


Book ID
119463384
Publisher
Elsevier Science
Year
1988
Tongue
English
Weight
722 KB
Volume
112
Category
Article
ISSN
1097-6833

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Fabry disease is an X-linked recessive inborn error of glycosphingolipid catabolism that results from the deficient activity of the lysosomal enzyme ␣-galactosidase A (␣-Gal A). A rapid, reliable, and universal linkage method was developed for molecular carrier detection and prenatal diagnosis. By d