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 | 2 |
Search Results
2 results
Results by year
Filters applied: . Clear all
Page 1
Clinical and genetic analysis of methylmalonic aciduria in 60 patients from Southern China: a single center retrospective study.
Orphanet J Rare Dis. 2024 May 15;19(1):198. doi: 10.1186/s13023-024-03210-0.
Orphanet J Rare Dis. 2024.
PMID: 38750596
Free PMC article.
Severe Zellweger spectrum disorder due to a novel missense variant in the PEX13 gene: A case report and the literature review.
Su L, Peng MZ, Chen XD, Wu S, Liu L.
Su L, et al.
Mol Genet Genomic Med. 2024 Jan;12(1):e2315. doi: 10.1002/mgg3.2315. Epub 2023 Nov 14.
Mol Genet Genomic Med. 2024.
PMID: 37962062
Free PMC article.
Item in Clipboard
Cite
Cite