MFN2 mutations cause severe phenotypes in most patients with CMT2A. (Q34999364)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | MFN2 mutations cause severe phenotypes in most patients with CMT2A. |
scientific article |
Statements
MFN2 mutations cause severe phenotypes in most patients with CMT2A (English)
S M E Feely
M Laura
C E Siskind
S Sottile
M Davis
V S Gibbons
20 April 2011
1 reference
1 reference