Cite
HARVARD Citation
Awano, H. et al. (2021). FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients. Journal of clinical neuroscience. pp. 215-221. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Awano, H. et al. (2021). FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients. Journal of clinical neuroscience. pp. 215-221. [Online].