Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1996 | 1 |
1998 | 1 |
2024 | 0 |
Search Results
2 results
Results by year
Filters applied: . Clear all
Page 1
Mice with an aspartylglucosaminuria mutation similar to humans replicate the pathophysiology in patients.
Hum Mol Genet. 1998 Feb;7(2):265-72. doi: 10.1093/hmg/7.2.265.
Hum Mol Genet. 1998.
PMID: 9425233
A mouse model for the human lysosomal disease aspartylglycosaminuria.
Kaartinen V, Mononen I, Voncken JW, Noronkoski T, Gonzalez-Gomez I, Heisterkamp N, Groffen J.
Kaartinen V, et al.
Nat Med. 1996 Dec;2(12):1375-8. doi: 10.1038/nm1296-1375.
Nat Med. 1996.
PMID: 8946839
Item in Clipboard
Cite
Cite