Sialuria: a follow-up report

Author:

Don N. A.,Wilcken B.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference3 articles.

1. Gahl, W. A., Renlund, M. and Thoene, J. G. Lysosomal transport disorders. In Scriver, C. R., Beaudet, A. L., Sly, W. S. and Valle, D. (eds.)The Metabolic Basis of Inherited Disease, 6th edn. McGraw Hill, New York, 1989, pp. 2640–2641

2. Seppala, R., Tietze, F., Weiss, P., Ashwell, G., Barsh, G. and Gahl, W. A. The metabolic defect in sialuria: lack of feedback control of uridine disphosphateN-acetylglucosamine 2-epimerase.Am. J. Hum. Genet. 45 (Suppl. 1) (1989) A11

3. Wilcken, B., Don, N., Greenaway, R., Hammond, J. and Sosula, L. Sialuria: A second case.J. Inher. Metab. Dis. 10 (1987) 97–99

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1. Sialuria-Related Intellectual Disability in Children and Adolescent of Pakistan: Tenth Patient Described has a Novel Mutation in the GNE Gene;CNS & Neurological Disorders - Drug Targets;2020-06-17

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3. S;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

4. Abnormal glycosylation with hypersialylated O-glycans in patients with Sialuria;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2006-06

5. Dominant Inheritance of Sialuria, an Inborn Error of Feedback Inhibition;The American Journal of Human Genetics;2001-06

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