Mosaicism for a pathogenic MFN2 mutation causes minimal clinical features of CMT2A in the parent of a severely affected child
Crossref DOI link: https://doi.org/10.1007/s10048-016-0504-2
Published Online: 2017-01-06
Published Print: 2017-01
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Schon, Katherine http://orcid.org/0000-0001-8054-8954
Spasic-Boskovic, Olivera
Brugger, Kim
Graves, Tracey D.
Abbs, Stephen
Park, Soo-Mi
Ambegaonkar, Gautam
Armstrong, Ruth
Funding for this research was provided by:
University of Cambridge
License valid from 2017-01-01