Found: 3
Select item for more details and to access through your institution.
Hereditary hyperferritinemia cataract syndrome in four patients with mutations in the IRE of the FTL gene.
- Published in:
- Clinical Genetics, 2013, v. 83, n. 5, p. 491, doi. 10.1111/j.1399-0004.2012.01934.x
- By:
- Publication type:
- Article
A homozygous mutation in the ferrochelatase gene underlies erythropoietic protoporphyria associated with palmar keratoderma.
- Published in:
- British Journal of Dermatology, 2009, v. 160, n. 6, p. 1330, doi. 10.1111/j.1365-2133.2009.09084.x
- By:
- Publication type:
- Article
Molecular heterogeneity of familial porphyria cutanea tarda in Spain: characterization of 10 novel mutations in the UROD gene.
- Published in:
- British Journal of Dermatology, 2007, v. 157, n. 3, p. 501, doi. 10.1111/j.1365-2133.2007.08064.x
- By:
- Publication type:
- Article