ASPARTYLGLYCOSAMINURIA IN NORTHERN NORWAY-Reference-Cited by-同舟云学术

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ASPARTYLGLYCOSAMINURIA IN NORTHERN NORWAY

Published:1976-05 Issue:7968 Volume:307 Page:1082-1083
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Borud O.,Torp K.H.

Publisher

Elsevier BV

Subject

General Medicine

Reference8 articles.

1. ASPARTYLGLYCOSAMINURIA

2. Detection of heterozygotes for aspartylglucosaminuria (AGU) in cultured fibroblasts

3. Aspartylglucosaminuria: Psychomotor retardation masquerading as a mucopolysaccharidosis

Cited by 5 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. Aspartylglycosaminuria: a review;Orphanet Journal of Rare Diseases;2016-12

2. Early clinical symptoms and incidence of aspartylglucosaminuria in Finland;Acta Paediatrica;1993-06

3. In vitro mutagenesis helps to unravel the biological consequences of aspartylglucosaminuria mutation;Genomics;1991-09

4. Measurement of aspartylglucosamine in physiological fluids with an amino acid analyzer: Fused peak analysis with dual photometers;Analytical Biochemistry;1981-09

5. Aspartylglycosaminuria in Northern Norway in eight patients: Clinical heterogeneity and variations with the diet;Journal of Inherited Metabolic Disease;1978-09

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