Mucopolysaccharidosis Type I
Mucopolysaccharidosis type I (MPS I) is caused by the deficiency of α-<span style="font-variant: small-caps;">l</span>-iduronidase, leading to the storage of dermatan and heparan sulfate. There is a broad phenotypical spectrum with the presence or absence of neurologic...
Main Authors: | , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2020-03-01
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Series: | Diagnostics |
Subjects: | |
Online Access: | https://www.mdpi.com/2075-4418/10/3/161 |