Aspartylglucosaminuria: Deficiency of aspartylglucosaminidase in cultured fibroblasts of patients and their heterozygous parents-Reference-Cited by-同舟云学术

Aspartylglucosaminuria: Deficiency of aspartylglucosaminidase in cultured fibroblasts of patients and their heterozygous parents

Published:2008-04-23 Issue:3 Volume:4 Page:297-300
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Aula P.,Näntöu V.,Laipio M.-L.,Autio S.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1973.tb01161.x/fullpdf

Reference13 articles.

1. Aspartylglucosaminuria. I. Fine structural studies on liver, kidney and brain;Arstila;Acta neuropath. (Berl.),1972

2. Autio , S. 1972 Aspartylglucosaminuria. Analysis of thirty-four patients J. ment. Defic. Res. 1 93

3. Autio , S. J. Visakorpi H. Järvinen 1973 Aspartylglucosaminuria (AGU): Further aspect of its clinical picture, epidemiology and mode of inheritance based on a series of 57 patients Ann. clin. Res.

4. The assay of arylculphatases A and B in human urine;Baum;Clin. chim. Acta,1959

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3. Aspartylglucosaminuria: Radiologic Course of the Disease With Histopathologic Correlation;Journal of Child Neurology;1997-09

4. Mutations causing aspartylglucosaminuria (AGU): A lysosomal accumulation disease;Human Mutation;1992

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