A novel hypomorphic PDX1 mutation responsible for permanent neonatal diabetes with subclinical exocrine deficiency.
Nicolino M; Claiborn KC; Senée V; Boland A; Stoffers DA; Julier C; Diabetes, 2010, vol. 59, issue 3, p 733, ISSN 1939327x. ISBN 1939327x.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef