Congenital central diabetes insipidus and optic atrophy in a Wolfram newborn: is there a role for WFS1 gene in neurodevelopment?
Crossref DOI link: https://doi.org/10.1186/s13052-014-0076-4
Published Online: 2014-09-26
Published Print: 2014-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Ghirardello, Stefano
Dusi, Elisa
Castiglione, Bianca
Fumagalli, Monica
Mosca, Fabio
License valid from 2014-09-26
Article History
Received: 20 May 2014
Accepted: 9 August 2014
First Online: 26 September 2014