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Description
Non-erythroid form of acute intermittent porphyria caused by promoter and frameshift mutations distant from the coding sequence of exon 1 of the HMBS gene

At this regard more evidences are necessary to better understand the interest of taurine for ensuring a proper muscle function in human other than in animals

doi: 10.1177/1933719112459234

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These symptoms are usually mild to moderate and tend to lessen over time
