Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:03829085n
Noun Concept
SYL
No term available
EN
Laminopathies are a group of rare genetic disorders caused by mutations in genes encoding proteins of the nuclear lamina. Wikipedia
Relations
Sources
IS A
EN
genetic disease

Please note that, in order to improve your browsing experience on this website, BabelNet® uses various types of cookies, including: browsing functionality, performance and statistical cookies.

By continuing to browse the site you are agreeing to our use of cookies. OK

License