Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study of 187 patients.

MLA

Baruteau, Julien, et al. “Clinical and Biological Features at Diagnosis in Mitochondrial Fatty Acid Beta-Oxidation Defects: A French Pediatric Study of 187 Patients.” Journal of Inherited Metabolic Disease, vol. 36, no. 5, Sept. 2013, pp. 795–803. EBSCOhost, https://doi.org/10.1007/s10545-012-9542-6.

APA

Baruteau, J., Sachs, P., Broué, P., Brivet, M., Abdoul, H., Vianey-Saban, C., & Ogier de Baulny, H. (2013). Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study of 187 patients. Journal of Inherited Metabolic Disease, 36(5), 795–803. https://doi.org/10.1007/s10545-012-9542-6

Chicago

Baruteau, Julien, Philippe Sachs, Pierre Broué, Michèle Brivet, Hendy Abdoul, Christine Vianey-Saban, and Hélène Ogier de Baulny. 2013. “Clinical and Biological Features at Diagnosis in Mitochondrial Fatty Acid Beta-Oxidation Defects: A French Pediatric Study of 187 Patients.” Journal of Inherited Metabolic Disease 36 (5): 795–803. doi:10.1007/s10545-012-9542-6.