Aspartylglucosaminuria in the United States-Reference-Cited by-同舟云学术

Aspartylglucosaminuria in the United States

Published:2008-04-23 Issue:6 Volume:23 Page:427-435
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Hreidarsson Stefan,Momas George H.,Valle David L.,Stevenson Roger E.,Taylor Harold,McCarty Joseph,Coker Steven B.,Green William R.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1983.tb01977.x/fullpdf

Reference25 articles.

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

2. Detection of heterozygotes for aspartylglucosaminuria (AGU) in cultured fibroblasts;Ada;Humangenetik,1974

3. Aspartylglucosaminuria: Deficiency of aspartyl-glucosaminidase in cultured fibroblasts of patients and their heterozygous parents;Ada;Clin. Genet.,1973

4. Enzymatic diagnosis and carrier detection of aspartylglucosaminuria using blood samples;Aula;Pediat. Res.,1976

5. Autio , S. 1982

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