Cite
HARVARD Citation
Morava, E. et al. (2016). ALG6‐CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies. Journal of inherited metabolic disease. 39 (5), pp. 713-723. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Morava, E. et al. (2016). ALG6‐CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies. Journal of inherited metabolic disease. 39 (5), pp. 713-723. [Online].