Identification and characterization of 40 novel hydroxymethylbilane synthase mutations that cause acute intermittent porphyria

Overview of attention for article published in Journal of Inherited Metabolic Disease, March 2018

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Identification and characterization of 40 novel hydroxymethylbilane synthase mutations that cause acute intermittent porphyria. https://t.co/pbqoHnh9uM https://t.co/NoptRxqqn6

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