DOI:
10.1055/s-00000041
Neuropediatrics
LinksClose Window
References
Choi BO, Nakhro K, Park HJ. , et al.
A cohort study of MFN2 mutations and phenotypic spectrums in Charcot-Marie-Tooth disease 2A patients.
Clin Genet 2015;
87 (06) 594-598
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.