Non-Neuropathic Form of Mucopolysaccharidosis Type II: Clinical Cases

Non-Neuropathic Form of Mucopolysaccharidosis Type II: Clinical Cases

Background. Mucopolysaccharidosis (MPS) type II is an X-linked hereditary disease from the lysosomal storage diseases group. The absence or malfunctioning of the iduronate-2-sulfatase enzyme leads to disruption in glycosaminoglycans (GAG) degradation. The GAG accumulation in lysosomes leads to dysfu...

Full description

Saved in:
Bibliographic Details
Main Authors: Nato D. Vashakmadze (Author), Natalia V. Zhurkova (Author), Leyla S. Namazova-Baranova (Author), Nina V. Fedorova (Author), Marina A. Babaykina (Author)
Format: Book
Published: "Paediatrician" Publishers LLC, 2021-03-01T00:00:00Z.
Subjects:
article
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available

Similar Items