Parisi, L., & Escher, R. Myopathy, lactic acidosis and sideroblastic anemia syndrome 1 (MLASA1): Clinical hallmarks in a large pedigree with a novel <i>PUS1</i> R144Q mutation, remarkable response to somatropin, and review of the literature. Ferrata Storti Foundation.
Chicago Style (17th ed.) CitationParisi, Lorenzo, and Robert Escher. Myopathy, Lactic Acidosis and Sideroblastic Anemia Syndrome 1 (MLASA1): Clinical Hallmarks in a Large Pedigree with a Novel <i>PUS1</i> R144Q Mutation, Remarkable Response to Somatropin, and Review of the Literature. Ferrata Storti Foundation.
MLA (9th ed.) CitationParisi, Lorenzo, and Robert Escher. Myopathy, Lactic Acidosis and Sideroblastic Anemia Syndrome 1 (MLASA1): Clinical Hallmarks in a Large Pedigree with a Novel <i>PUS1</i> R144Q Mutation, Remarkable Response to Somatropin, and Review of the Literature. Ferrata Storti Foundation.