Manage settings
MENU
About this site
In het Nederlands
Home
Researchers
Projects
Organisations
Publications
Contact
Research Explorer
Your browser does not support JavaScript or JavaScript is not enabled. Without JavaScript some functions of this webapplication may be disabled or cause error messages. To enable JavaScript, please consult the manual of your browser or contact your system administrator.
Researcher
Maxim Verlee
Profile
Projects
Publications
Activities
Awards & Distinctions
1
Result
2021
Loss-of-function variants in EFEMP1 cause a recognizable connective tissue disorder characterized by cutis laxa and multiple herniations
Maxim Verlee
Aude Beyens
Alper Gezdirici
Elif Gulec
Lore Pottie
Silke De Feyter
Michiel Vanhooydonck
Piyanoot Tapaneeyaphan
Sofie Symoens
Bert Callewaert
A1
Journal Article
in
GENES
2021