Balasubramaniam, S., Lewis, B., Mock, D. M., Said, H. M., Tarailo-Graovac, M., Mattman, A., . . . Christodoulou, J. (2016). Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD). JIMD Rep.
Citação norma ChicagoBalasubramaniam, Shanti, et al. "Leigh-Like Syndrome Due to Homoplasmic M.8993T>G Variant With Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD)." JIMD Rep 2016.
MLA citiranjeBalasubramaniam, Shanti, et al. "Leigh-Like Syndrome Due to Homoplasmic M.8993T>G Variant With Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD)." JIMD Rep 2016.