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PedAM

Pediatric Disease Annotations & Medicines




Disease liver disease
Phenotype C0268483|tyrosinemia
Sentences 1
PubMedID- 26088193 The derivation of ipscs from somatic cells of patients with liver diseases, including tyrosinemia, glycogen storage disease, progressive familial hereditary cholestasis, and crigler-najjar syndrome (two siblings), through retroviral transduction of yamanaka’s factors in serum and feeder-free culture conditions has been shown (ghodsizadeh et al., 2010).

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