Associated Papers
Distinct functional consequences of ECEL1/DINE missense mutations in the pathogenesis of congenital contracture disorders.
Nagata K et al.
Acta Neuropathologica Communications, 2017
ECEL1 mutation causes fetal arthrogryposis multiplex congenita.
Dohrn N et al.
American Journal of Medical Genetics. Part A, 2015
Expanding the phenotypic spectrum of ECEL1-related congenital contracture syndromes.
Shaaban S et al.
Clinical Genetics, 2014
The neuronal endopeptidase ECEL1 is associated with a distinct form of recessive distal arthrogryposis.
Dieterich K et al.
Human Molecular Genetics, 2013
Select a paper to view details