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A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype

A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype

Iapadre, Giulia; Morana, Giovanni; Vari, Maria Stella; Pinto, Francesca; Lanteri, Paola; Tessa, Alessandra; Santorelli, Filippo Maria; Striano, Pasquale; Verrotti, Alberto
  • 期刊名称European Journal of Paediatric Neurology
  • 作者Iapadre, Giulia; Morana, Giovanni; Vari, Maria Stella; Pinto, Francesca; Lanteri, Paola; Tessa, Alessandra; Santorelli, Filippo Maria; Striano, Pasquale; Verrotti, Alberto
  • 印刷ISSN1090-3798
  • 文件大小1009.28KB
  • 发表时间2018-1
  • DOI10.1016/j.ejpn.2017.12.020
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