Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders
Harjot K. Saini-Chohan(Amsterdam UMC Location University of Amsterdam), Grant M. Hatch(University of Manitoba), Frédéric M. Vaz(Netherlands Metabolomics Centre), Ryan W. Mitchell(Amsterdam UMC Location University of Amsterdam), Teresa Zelinski(Research Manitoba)
Cited by 53
Related Papers
Modeling the mitochondrial cardiomyopathy of Barth syndrome with induced pluripotent stem cell and heart-on-chip technologies
|Nature Medicine|2014|843
Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood
|The American Journal of Human Genetics|2008|218
Deficiency of Innate and Acquired Immunity Caused by an <i>IKBKB</i> Mutation
|New England Journal of Medicine|2013|184
Blood group terminology 2004: from the International Society of Blood Transfusion committee on terminology for red cell surface antigens
|Vox Sanguinis|2004|180
Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosis
|Journal of Lipid Research|2005|144