Cite
HARVARD Citation
Torraco, A. et al. (2017). A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemia. Clinical genetics. 91 (3), pp. 441-447. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Torraco, A. et al. (2017). A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemia. Clinical genetics. 91 (3), pp. 441-447. [Online].