Title: | MFN2 mutations cause severe phenotypes in most patients with CMT2A |
Journal : | Neurology, 76, 20 |
Authors: | Feely SME ; Laura M ; Siskind CE ; Sottile S ; Davis M ; Gibbons VS ; Reilly M ; Shy ME |
Material Type: | Article |
Publication Date: | 2011 |
Size: | p. 1690-1696 |
Languages: | English |
Keywords : | adulthood ; children ; CMT2A2 ; CMTNS ; cohort studies ; electrodiagnosis ; genetic mutations ; MFN2 gene ; MRI ; phenotypes ; research prospects ; teenagers ; young adults |
Abstract: |
Accès au résumé PubMed / to PubMed abstract |
Lien associé : | http://www.ncbi.nlm.nih.gov/pubmed/21508331 |
Pubmed / DOI : | DOI : 10.1212/WNL.0b013e31821a441e |