Aspartylglycosaminuria: protein chemistry and molecular biology of the most common lysosomal storage disorder of glycoprotein degradation-Reference-Cited by-同舟云学术

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Aspartylglycosaminuria: protein chemistry and molecular biology of the most common lysosomal storage disorder of glycoprotein degradation

Published:1993-10 Issue:13 Volume:7 Page:1247-1256
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

Mononen Ilkka¹,Fisher Krishna J.²,Kaartinen Vesa¹³,Aronson Nathan N.⁴

Affiliation:

1. Department of Clinical ChemistryUniversity of Kuopio, and Center for Diagnostic BiotechnologyA. I. Virtanen InstituteSF‐70210KuopioFinland

2. The Institute for Human Gene TherapyThe Wistar InstitutePhiladelphiaPennsylvania19104‐4268USA

3. Department of Pathology and Laboratory MedicineChildren's Hospital of Los AngelesLos AngelesCalifornia90054‐0700USA

4. Department of BiochemistryUniversity of South AlabamaMobileAlabama36688USA

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fasebj.7.13.8405810

Cited by 60 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

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2. A 37-Year-Old Man With Intellectual Disability Discovered to Have Aspartylglucosaminuria;Neurology Genetics;2024-06

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