Congenital central diabetes insipidus and optic atrophy in a Wolfram newborn: is there a role for WFS1 gene in neurodevelopment? - Concepedia

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Congenital central diabetes insipidus and optic atrophy in a Wolfram newborn: is there a role for WFS1 gene in neurodevelopment?

DOI Full Paper Access

13

Citations

24

References

2014

Year

Stefano Ghirardello, Elisa Dusi, Bianca Castiglione, Monica Fumagalli, Fabio Mosca

The Italian Journal of Pediatrics/Italian journal of pediatrics

References

	Year	Citations

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