Use of Retinoids in Congenital Erythropoietic Porphyria
Zebrafish model of CEP develops bone phenotype resembling human disease
Congenital erythropoietic porphyria (CEP) is a rare genetic disorder leading to accumulation of uro/coproporphyrin-I (uro-I) in tissues due to inhibition of the enzyme uroporphyrinogen-III synthase. Clinical manifestations of CEP include bone fragility,...
Inventor(s): Bishr Omary
Category(s): Technology Classifications > Therapeutics