Related references
Note: Only part of the references are listed.Wolcott-Rallison syndrome associated with congenital malformations and a mosaic deletion 15q 11-12
F.J. Stewart et al.
CLINICAL GENETICS (2010)
Wolcott-Rallison syndrome
Cecile Julier et al.
ORPHANET JOURNAL OF RARE DISEASES (2010)
A novel mutation in the EIF2AK3 gene with variable expressivity in two patients with Wolcott-Rallison syndrome
F. Durocher et al.
CLINICAL GENETICS (2006)
Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3
S Brickwood et al.
JOURNAL OF MEDICAL GENETICS (2003)
EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome
M Delépine et al.
NATURE GENETICS (2000)