DOI:
10.1055/s-00000041
Neuropediatrics
LinksClose Window
References
Kollberg G, Darin N, Benan K. , et al.
A novel homozygous RRM2B missense mutation in association with severe mtDNA depletion.
Neuromuscul Disord 2009;
19 (02) 147-150
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.