APA

Balasubramaniam S., Lewis B., Mock D. M., Said H. M., Tarailo-Graovac M., Mattman A., van Karnebeek C. D., Thorburn D. R., Rodenburg R. J. & Christodoulou J. (2017). Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD). : JIMD reports.

Chicago

Balasubramaniam Shanti, Lewis B, Mock D M, Said H M, Tarailo-Graovac M, Mattman A, van Karnebeek C D, Thorburn D R, Rodenburg R J and Christodoulou J. 2017. Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD). : JIMD reports.

Harvard

Balasubramaniam S., Lewis B., Mock D. M., Said H. M., Tarailo-Graovac M., Mattman A., van Karnebeek C. D., Thorburn D. R., Rodenburg R. J. and Christodoulou J. (2017). Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD). : JIMD reports.

MLA

Balasubramaniam Shanti, Lewis B, Mock D M, Said H M, Tarailo-Graovac M, Mattman A, van Karnebeek C D, Thorburn D R, Rodenburg R J and Christodoulou J. Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD). : JIMD reports. 2017.