Pages that link to "Q44325127"
Jump to navigation
Jump to search
The following pages link to Novel mutations and phenotypic effect of the splice site modulator IVS3-48C in nine Swedish families with erythropoietic protoporphyria (Q44325127):
Displaying 12 items.
- Erythropoietic protoporphyria (Q21202891) (← links)
- Erythropoietic protoporphyria in Sweden: demographic, clinical, biochemical and genetic characteristics (Q34111563) (← links)
- The incidence of inherited porphyrias in Europe (Q34309198) (← links)
- Contribution of a common single-nucleotide polymorphism to the genetic predisposition for erythropoietic protoporphyria (Q34563770) (← links)
- Liver disease in erythropoietic protoporphyria: insights and implications for management (Q36759851) (← links)
- Novel null-allele mutations and genotype-phenotype correlation in Argentinean patients with erythropoietic protoporphyria (Q37310958) (← links)
- Antisense oligonucleotide-based therapy in human erythropoietic protoporphyria (Q37693360) (← links)
- Treatment options in acute porphyria, porphyria cutanea tarda, and erythropoietic protoporphyria (Q41941579) (← links)
- Functional associations of genetic variants involved in the clinical manifestation of erythropoietic protoporphyria in the Argentinean population (Q47757083) (← links)
- Genotypic determinants of phenotype in North American patients with erythropoietic protoporphyria (Q48223265) (← links)
- Erythropoietic protoporphyria a clinical and molecular study from Lebanon: Ferrochelatase a potential tumor suppressor gene in colon cancer. (Q48364515) (← links)
- Incomplete erythropoietic protoporphyria caused by a splice site modulator homozygous IVS3-48C polymorphism in the ferrochelatase gene. (Q55059261) (← links)