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47. Co-existence of two functional mutations on the same allele of the human ferrochelatase gene in erythropoietic protoporphyria. Di Pierro E; Brancaleoni V; Moriondo V; Besana V; Cappellini MD Clin Genet; 2007 Jan; 71(1):84-8. PubMed ID: 17204051 [TBL] [Abstract][Full Text] [Related]
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56. [McArdle disease: a disease with high allele heterogeneity with different physiopathologic mechanism]. Gámez J Neurologia; 2000 Apr; 15(4):147-51. PubMed ID: 10846881 [No Abstract] [Full Text] [Related]
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