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 |
---|---|
2008 | 1 |
2021 | 1 |
2024 | 0 |
Search Results
2 results
Results by year
Filters applied: . Clear all
Page 1
Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy.
J Clin Endocrinol Metab. 2008 Apr;93(4):1129-34. doi: 10.1210/jc.2007-1328. Epub 2008 Jan 22.
J Clin Endocrinol Metab. 2008.
PMID: 18211975
Free article.
Biallelic CAV1 null variants induce congenital generalized lipodystrophy with achalasia.
Karhan AN, Zammouri J, Auclair M, Capel E, Apaydin FD, Ates F, Verpont MC, Magré J, Fève B, Lascols O, Usta Y, Jéru I, Vigouroux C.
Karhan AN, et al.
Eur J Endocrinol. 2021 Nov 10;185(6):841-854. doi: 10.1530/EJE-21-0915.
Eur J Endocrinol. 2021.
PMID: 34643546
Item in Clipboard
Cite
Cite