B. Aral
Laboratoire de Biochimie Médicale B
CNRS, URA1335
Institut Necker
France
Name/email consistency: high
- Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosis. Aral, B., Benelli, C., Ait-Ghezala, G., Amessou, M., Fouque, F., Maunoury, C., Créau, N., Kamoun, P., Marsac, C. Am. J. Hum. Genet. (1997)