![](/img/cover-not-exists.png)
The first founder DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome
N. Brahimi, M. Jambou, E. Sarzi, V. Serre, N. Boddaert, S. Romano, P. de Lonlay, A. Slama, A. Munnich, A. Rötig, J.P. Bonnefont, A.S. LebreVolume:
97
Year:
2009
Language:
english
DOI:
10.1016/j.ymgme.2009.03.007
File:
PDF, 894 KB
english, 2009