DOI:
10.1055/s-00000034
Klinische Pädiatrie
LinksClose Window
References
Rochow N, Bachmaier N, Tost F et al.
The case of a 1-year-old girl with hereditary hyperferritinemia cataract syndrome.
Pediatr Hematol Oncol 2009;
26: 136-141
We do not assume any responsibility for the contents of the web pages of other providers.