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 |
---|---|
2021 | 1 |
2022 | 1 |
2025 | 1 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Page 1
Bi-allelic loss of function variants in GOLGA2 are associated with a complex neurological phenotype: Report of a second family.
Clin Genet. 2021 Dec;100(6):748-751. doi: 10.1111/cge.14053. Epub 2021 Aug 29.
Clin Genet. 2021.
PMID: 34424553
Removal of MuRF1 Increases Muscle Mass in Nemaline Myopathy Models, but Does Not Provide Functional Benefits.
Lindqvist J, Kolb J, de Winter J, Tonino P, Hourani Z, Labeit S, Ottenheijm C, Granzier H.
Lindqvist J, et al.
Int J Mol Sci. 2022 Jul 23;23(15):8113. doi: 10.3390/ijms23158113.
Int J Mol Sci. 2022.
PMID: 35897687
Free PMC article.
Item in Clipboard
A Splice Site Variant in SENP7 Results in a Severe Form of Arthrogryposis.
Kotecha U, Kim ES, Shah PS, Shah N, Gupta VA.
Kotecha U, et al.
Clin Genet. 2025 Jan 4. doi: 10.1111/cge.14698. Online ahead of print.
Clin Genet. 2025.
PMID: 39754459
Item in Clipboard
Cite
Cite
ARTICLE TYPE
ARTICLE LANGUAGE
AGE
Filters on the sidebar will be reset to the default list and any currently applied filters will be cleared.