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MFN2 mutations cause severe phenotypes in most patients with CMT2A.
- Source :
- Neurology; 5/17/2011, Vol. 76 Issue 20, p1690-1696, 7p
- Publication Year :
- 2011
Details
- Language :
- English
- ISSN :
- 00283878
- Volume :
- 76
- Issue :
- 20
- Database :
- Supplemental Index
- Journal :
- Neurology
- Publication Type :
- Academic Journal
- Accession number :
- 104903801
- Full Text :
- https://doi.org/10.1212/WNL.0b013e31821a441e