Clinical course and biochemistry of sialuria

Author:

Enns G. M.12,Seppala R.34,Musci T. J.5,Weisiger K.2,Ferrell L. D.6,Wenger D. A.7,Gahl W. A.3,Packman S.2

Affiliation:

1. ; Division of Medical Genetics, Department of Pediatrics; Stanford University; California

2. ; Division of Medical Genetics, Department of Pediatrics; University of California; San Francisco California

3. ; Section on Human Biochemical Genetics, Heritable Disorders Branch, National Institute of Child Health and Human Development; National Institutes of Health; Maryland USA

4. ; Department of Pathology; Oulu University; Oulu Finland

5. ; Department of Obstetrics and Gynecology; USA

6. ; Department of Pathology; University of California; San Francisco California

7. ; Department of Neurology; Jefferson Medical College; Philadelphia Pennsylvania USA

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference17 articles.

1. Sialuria: a follow-up report;Don;J Inherit Metab Dis,1991

2. Sialuria in a Portuguese girl: clinical, biochemical and molecular characteristics;Ferreira;Mol Genet Metab,1999

3. La sialurie: un trouble métabolique original;Fontaine;Helv Paediatr Acta (Suppl. XVII),1968

4. The feedback control of sugar nucleotide biosynthesis in liver;Kornfeld;Proc Natl Acad Sci USA,1964

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