Metachromatic leukodystrophy. I. Prenatal detection of arylsulphatase A deficiency.

Clinical genetics ·Vol. 4 ·No. 3 ·1973-00-00 ·Pages 256-9

van der Hagen CB, Borresen AL, Molne K, Oftedal G, Bjoro K, Berg K

Abstract

暂无摘要

MeSH Terms

Adult Amniocentesis Amniotic Fluid/cytology,enzymology Biopsy Catechols Cells, Cultured Child, Preschool Female Fetus/enzymology Fibroblasts/enzymology Gestational Age Humans Leukodystrophy, Metachromatic/diagnosis,enzymology Male Nitro Compounds Pregnancy Prenatal Diagnosis Skin/pathology Sulfatases/metabolism

Chemicals

Catechols Nitro Compounds Sulfatases

Authors & Affiliations

6 authors, click to expand affiliations / ORCID

van der Hagen C B

Borresen A L

Molne K

Oftedal G

Bjoro K

Berg K

Article Info

Journal

Clinical genetics

Abbr.

Clin Genet

ISSN

0009-9163

Published

1973-00-00

Pages

256-9

Language

English

Region

Denmark

NLM ID

0253664

Subset

External Links

PubMed source View journal details

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Metachromatic leukodystrophy. I. Prenatal detection of arylsulphatase A deficiency.

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