Maternal uniparental disomy of chromosome 2 in a patient with a DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome

MLA

Haudry, Coralie, et al. “Maternal Uniparental Disomy of Chromosome 2 in a Patient with a DGUOK Mutation Associated with Hepatocerebral Mitochondrial DNA Depletion Syndrome.” Molecular Genetics & Metabolism, vol. 107, no. 4, Dec. 2012, pp. 700–04. EBSCOhost, https://doi.org/10.1016/j.ymgme.2012.10.008.

APA

Haudry, C., de Lonlay, P., Malan, V., Bole-Feysot, C., Assouline, Z., Pruvost, S., Brassier, A., Bonnefont, J.-P., Munnich, A., Rötig, A., & Lebre, A.-S. (2012). Maternal uniparental disomy of chromosome 2 in a patient with a DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome. Molecular Genetics & Metabolism, 107(4), 700–704. https://doi.org/10.1016/j.ymgme.2012.10.008

Chicago

Haudry, Coralie, Pascale de Lonlay, Valerie Malan, Christine Bole-Feysot, Zahra Assouline, Solenn Pruvost, Anais Brassier, et al. 2012. “Maternal Uniparental Disomy of Chromosome 2 in a Patient with a DGUOK Mutation Associated with Hepatocerebral Mitochondrial DNA Depletion Syndrome.” Molecular Genetics & Metabolism 107 (4): 700–704. doi:10.1016/j.ymgme.2012.10.008.