Metachromatic leukodystrophy: Molecular genetics and an animal model-Reference-Cited by-同舟云学术

Metachromatic leukodystrophy: Molecular genetics and an animal model

Published:1998-08 Issue:5 Volume:21 Page:564-574
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Gieselmann V.¹,Matzner U.¹,Hess B.¹,Lüllmann-Rauch R.²,Coenen R.²,Hartmann D.²,D'Hooge R.³⁴,Dedeyn P.³,Nagels G.³

Affiliation:

1. ; Biochemisches Institut der Christian-Albrechts-Universität zu Kiel; Kiel Germany

2. ; Anatomisches Institut der Christian-Albrechts-Universität zu Kiel; Kiel Germany

3. Laboratory of Neurochemistry and Behaviour; University Instelling; Belgium

4. ; Born-Bunge Foundation; University of Antwerp; Antwerp Belgium

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005471106088/fullpdf

Reference49 articles.

1. Molecular analysis of Hurler syndrome in Druze and Muslim Arab patients: multiple allelic mutations of the IDUA gene in a small geographic area;Bach;Am J Hum Genet,1993

2. Prevalence of common mutations in the arylsulfatase A gene in metachromatic leukodystrophy patients diagnosed in Great Britain;Barth;Hum Genet,1993

3. Missense mutations in the arylsulfatase A gene of metachromatic leukodystrophy patients;Barth;Hum Mol Genet,1993

4. Frequency of arylsulfatase A pseudo-deficiency associated mutations in a healthy population;Barth;J Med Genet,1994

5. Identification of seven novel mutations associated with metachromatic leukodystrophy;Barth;Hum Mutat,1995

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