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 |
---|---|
2023 | 1 |
2024 | 1 |
Search Results
2 results
Results by year
Filters applied: . Clear all
Page 1
A compound heterozygous mutation of ERCC8 is responsible for a family with Cockayne syndrome.
Mol Biol Rep. 2024 Feb 27;51(1):371. doi: 10.1007/s11033-024-09235-9.
Mol Biol Rep. 2024.
PMID: 38411728
Late-onset hereditary spastic paraplegia associated with a genetic variant in interferon induced with helicase c domain 1 (IFIH1) gene.
Zhang SY, Zhu L, Fan LL, Xiang R, Zeng L, Jin JY.
Zhang SY, et al.
QJM. 2023 Jul 28;116(7):574-576. doi: 10.1093/qjmed/hcad055.
QJM. 2023.
PMID: 37040079
No abstract available.
Item in Clipboard
Cite
Cite