![](/img/cover-not-exists.png)
Respiratory chain complex I deficiency due to NDUFA12 mutations as a new cause of Leigh syndrome
Ostergaard, E., Rodenburg, R. J., van den Brand, M., Thomsen, L. L., Duno, M., Batbayli, M., Wibrand, F., Nijtmans, L.Volume:
48
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmg.2011.088856
Date:
November, 2011
File:
PDF, 234 KB
english, 2011