Phenotypic spectrum of Salla disease, a free sialic acid storage disorder-Reference-Cited by-同舟云学术

Phenotypic spectrum of Salla disease, a free sialic acid storage disorder

Published:2002-04 Issue:4 Volume:26 Page:267-273
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Varho Tarja T.,Alajoki Liisa E.,Posti Kristiina M.,Korhonen Tapio T.,Renlund Martin G.,Nyman Samuel R.G.,Sillanpää Matti L.,Aula Pertti P.

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference37 articles.

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3. Defective sialic acid egress from isolated fibroblast lysosomes of patients with Salla disease;Renlund;Science,1986

4. Characterization of a proton-driven carrier for sialic acid in the lysosomal membrane;Mancini;Evidence for a group-specific transport system for acidic monosaccarides. J Biol Chem,1989

5. The genetic locus of free sialic acid storage disease maps to the long arm of chromosome 6;Haataja;Am J Hum Genet,1994

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