Molecular basis of variant pseudo-Hurler polydystrophy (mucolipidosis IIIC)-Reference-Cited by-同舟云学术

Molecular basis of variant pseudo-Hurler polydystrophy (mucolipidosis IIIC)

Published:2000-03-01 Issue:5 Volume:105 Page:673-681
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Raas-Rothschild Annick,Cormier-Daire Valerie,Bao Ming,Genin Emmanuelle,Salomon Remi,Brewer Kevin,Zeigler Marsha,Mandel Hanna,Toth Steve,Roe Bruce,Munnich Arnold,Canfield William M.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference35 articles.

1. Mutant Enzymatic and Cytological Phenotypes in Cultured Human Fibroblasts

2. A hypothesis for I-cell disease: Defective hydrolases that do not enter lysosomes

3. A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts

4. Phosphohexosyl components of a lysosomal enzyme are recognized by pinocytosis receptors on human fibroblasts.

5. Trafficking of lysosomal enzymes 1

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