Fatal Rhabdomyolysis in 2 Children with LPIN1 Mutations

Michot, 2010, LPIN1 gene mutations: a major cause of severe rhabdomyolysis in early childhood, Hum Mutat, 31, E1564, 10.1002/humu.21282

Zeharia, 2008, Mutations in LPIN1 cause recurrent acute myoglobinuria in childhood, Am J Hum Genet, 83, 489, 10.1016/j.ajhg.2008.09.002

Slovis, 2002, ABCs of clinical electrocardiography: conditions not primarily affecting the heart, BMJ, 324, 1320, 10.1136/bmj.324.7349.1320

Han, 2006, The Saccharomyces cerevisiae Lipin homolog is a Mg2+-dependent phosphatidate phosphatase enzyme, J Biol Chem, 281, 9210, 10.1074/jbc.M600425200

Mitra, 2011, Cardiac lipin 1 expression is regulated by the peroxisome proliferator activated receptor γ coactivator 1α/estrogen related receptor axis, J Mol Cell Cardiol, 51, 120, 10.1016/j.yjmcc.2011.04.009

Kok, 2012, Relationship of glucose and oleate metabolism to cardiac function in lipin-1–deficient (fld) mice, J Lipid Res, 53, 105, 10.1194/jlr.M019430

Chatzizisis, 2008, The syndrome of rhabdomyolysis: complications and treatment, Eur J Intern Med, 19, 568, 10.1016/j.ejim.2007.06.037

Gunal, 2004, Early and vigorous fluid resuscitation prevents acute renal failure in the crush victims of catastrophic earthquakes, J Am Soc Nephrol, 15, 1862, 10.1097/01.ASN.0000129336.09976.73