Inheritance, Biochemical Abnormalities, and Clinical Features of Feline Mucolipidosis II: The First Animal Model of Human I-Cell Disease
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,Biotechnology
Link
http://academic.oup.com/jhered/article-pdf/94/5/363/6454076/esg080.pdf
Cited by 37 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. Mucolipidoses Overview: Past, Present, and Future;International Journal of Molecular Sciences;2020-09-17
2. Upregulation of Sortilin, a Lysosomal Sorting Receptor, Corresponds with Reduced Bioavailability of Latent TGFβ in Mucolipidosis II Cells;Biomolecules;2020-04-26
3. Large animal models contribute to the development of therapies for central and peripheral nervous system dysfunction in patients with lysosomal storage diseases;Human Molecular Genetics;2019-08-06
4. Characterization of mesenchymal stem cells in mucolipidosis type II (I-cell disease);TURKISH JOURNAL OF BIOLOGY;2019-06-13
5. A GNPTAB nonsense variant is associated with feline mucolipidosis II (I-cell disease);BMC Veterinary Research;2018-12
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