Sphingolipidoses in Turkey
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health
Reference23 articles.
1. Lysosomal storage diseases;Neufeld;Annu Rev Biochem,1991
2. Disorders of sphingolipid metabolism;Barth,2000
3. Biochemical basis of late-onset neurolipidoses;Conzelmann;Dev Neurosci,1991
4. Quantitative correlation between the residual activity of β-hexosaminidase A and arylsulfatase A and the severity of the resulting lysosomal storage disease;Leinekugel;Hum Genet,1992
5. A study on enzyme activities of some sphingolipidoses;Özkara;Turk J Pediatr,1994
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