학술논문
Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3
Document Type
Periodical
Author
Source
Journal of Medical Genetics. September 2003, Vol. 40 Issue 9, p685, 5 p.
Subject
Language
English
ISSN
0022-2593
Abstract
Wolcott-Rallison syndrome (OMIM 226980) is a rare autosomal recessive disorder characterised by permanent insulin requiring diabetes developing in the newborn period or early infancy, an early tendency to skeletal fractures, [...]