Molecular analysis of LPIN1 in Jordanian patients with rhabdomyolysisSaied Ali Jaradat, Wajdi Amayreh, Kefah Al-Qa'qa', Jan KrayyemMeta gene2016Recessive mutations in LPIN1, which encodes a phosphatidate phosphatase enzyme, are a frequent cause of severe rhabdomyolysis in childhood. Hence, we sequenced the 19 coding exons of the gene in… (More)