Phenotype Correction in Murine Mucopolysaccharidosis Type VII by Transplantation of Human Amniotic Epithelial Cells after Adenovirus-Mediated Gene Transfer
Cell therapy with human amniotic epithelial (HAE) cells was developed as an alternative method for enzyme replacement therapy in congenital lysosomal storage disorders, but only limited therapeutic efficacy has been reported. A major drawback is insufficient production and secretion of lysosomal enz...
Main Authors: | , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
SAGE Publishing
2000-09-01
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Series: | Cell Transplantation |
Online Access: | https://doi.org/10.1177/096368970000900515 |