DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
LinksClose Window
References
Mechler K, Mountford WK, Hoffmann GF, Ries M.
Ultra-orphan diseases: a quantitative analysis of the natural history of molybdenum cofactor deficiency.
Genet Med 2015;
17 (12) 965-970
We do not assume any responsibility for the contents of the web pages of other providers.