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1. Identification of two novel PBGD mutations in acute intermittent porphyria patients accompanying anemia in mainland China.

Author

Liu G, Li X, Shu H, Hu YL, Anderson G, Qian J, and Nie G

Subjects
Anemia complications, Anemia pathology, China, Female, Humans, Mutation, Porphyria, Acute Intermittent complications, Porphyria, Acute Intermittent pathology, White People genetics, Young Adult, Anemia genetics, Asian People genetics, Hydroxymethylbilane Synthase genetics, Porphyria, Acute Intermittent genetics
Published
2011
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