TY  - RPRT
TI  - Mitochondrial fusion defects caused by CMT2A disease-associated variants of Mfn2
AU  - Samanas, N. B.
AU  - Engelhart, E. A.
AU  - Hoppins, S.
PY  - 2019
DO  - 10.1101/651877
UR  - https://www.biorxiv.org/content/10.1101/651877v1
ID  - 10.1101/651877
ER  -