| Title: |
A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype |
| Authors: |
Iapadre G; Morana G; Vari MS; Pinto F; Lanteri P; Tessa A; Santorelli FM; Striano P; Verrotti A |
| Contributors: |
Iapadre G; Morana G; Vari MS; Pinto F; Lanteri P; Tessa A; Santorelli FM; Striano P; Verrotti A |
| Publication Year: |
2018 |
| Collection: |
Università degli studi di Torino: AperTo (Archivio Istituzionale ad Accesso Aperto) |
| Document Type: |
article in journal/newspaper |
| Language: |
English |
| Relation: |
info:eu-repo/semantics/altIdentifier/wos/WOS:000431161700033; volume:22; firstpage:563; lastpage:567; numberofpages:5; journal:EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY; http://hdl.handle.net/2318/1752320; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85040544559 |
| DOI: |
10.1016/j.ejpn.2017.12.020 |
| Availability: |
http://hdl.handle.net/2318/1752320; https://doi.org/10.1016/j.ejpn.2017.12.020 |
| Rights: |
info:eu-repo/semantics/closedAccess |
| Accession Number: |
edsbas.C73AD70A |
| Database: |
BASE |