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Researcher
Michiel Vanhooydonck
Profile
Projects
Publications
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2
Results
2021
Loss of zebrafish atp6v1e1b, encoding a subunit of vacuolar ATPase, recapitulates human ARCL type 2C syndrome and identifies multiple pathobiological signatures
Lore Pottie
Wouter Van Gool
Michiel Vanhooydonck
Franz-Georg Hanisch
Geert Goeminne
Andreja Rajkovic
Paul Coucke
Patrick Sips
Bert Callewaert
A1
Journal Article
in
PLOS GENETICS
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