The I-Cell model: the molecular basis for abnormal lysosomal enzyme transport in mucolipidosis II and mucolipidosis III

Author:

Sly William S.,Sundaram Vasantha

Publisher

Elsevier

Reference92 articles.

1. Prenatal diagnosis and fetal pathology of I-cell disease (mucolipidosis type II);AULA;Journal of Pediatrics,1975

2. Deficiency of extracellular hydrolase phosphorylation;BACH;Biochemical and Biophysical Research Communications,1979

3. The mannose-6-phosphate receptor for lysosomal enzymes is concentrated in cis Golgi cisternae;BROWN;Cell,1984

4. Gargoylism (Hunter-Hurler disease, dysostosis multiplex, lipochondrodystrophy): prenatal and neonatal bone lesions and their early postnatal evolution;CAFFEY;American Journal of Roentgenology,1952

5. Neonatal mucolipidosis II (I-cell disease): clinical, radiological and biochemical studies in a case;CIPOLLONI;Helvetica Paediatrica Acta,1980

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The natural history and osteodystrophy of mucolipidosis types II and III;Journal of Paediatrics and Child Health;2010-03-29

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