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Dominant GDAP1 mutations cause predominantly mild CMT phenotypes.
- Source :
- Neurology; 8/9/2011, Vol. 77 Issue 6, p540-548, 9p
- Publication Year :
- 2011
Details
- Language :
- English
- ISSN :
- 00283878
- Volume :
- 77
- Issue :
- 6
- Database :
- Supplemental Index
- Journal :
- Neurology
- Publication Type :
- Academic Journal
- Accession number :
- 108249315
- Full Text :
- https://doi.org/10.1212/WNL.0b013e318228fc70