Variable onset of metachromatic leukodystrophy in a Vietnamese family-Reference-Cited by-同舟云学术

Variable onset of metachromatic leukodystrophy in a Vietnamese family

Published:2000-08 Issue:2 Volume:23 Page:173-176
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Arbour Laura T,Silver Kenneth,Hechtman Peter,Treacy Eileen P,Coulter-Mackie Marion B

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference13 articles.

1. Kolodny EH, Fluharty AL. Metachromatic leukodystrophy and multiple sulfatase deficiency: Sulfatide lipidosis. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The metabolic and molecular bases of inherited disease, 7th ed. New York: McGraw-Hill, 1995;2:2693–739.

2. Occurrence, distribution, and phenotype of arylsulfatase A mutations in patients with metachromatic leukodystrophy;Berger;Am J Med Genet,1997

3. Commentary;Thomas;Am J Hum Genet,1994

4. Arylsulfatase A pseudodeficiency;Gieselmann;Proc Natl Acad Sci USA,1989

5. DNA based diagnosis of arylsulfatase A deficiencies as a supplement to enzyme assay;Coulter-Mackie;Clin Biochem,1997

Cited by 23 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Case Report: Novel Arylsulfatase A (ARSA) Gene Mutations in a Patient With Adult-Onset Metachromatic Leukodystrophy Misdiagnosed as Multiple Sclerosis;Frontiers in Neurology;2021-01-11

2. Lysosomal Storage Disorders;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2021

3. Chinese Cases of Metachromatic Leukodystrophy with the Novel Missense Mutations in ARSA Gene;Journal of Molecular Neuroscience;2020-07-02

4. Metachromatic leukodystrophy and multiple sulfatase deficiency;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020

5. Phenotypic variation between siblings with Metachromatic Leukodystrophy;Orphanet Journal of Rare Diseases;2019-06-11