A cohort study of MFN2 mutations and phenotypic spectrums in Charcot–Marie–Tooth disease 2A patients

Publisher: John Wiley & Sons Inc

E-ISSN: 1399-0004|87|6|594-598

ISSN: 0009-9163

Source: CLINICAL GENETICS, Vol.87, Iss.6, 2015-06, pp. : 594-598

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Abstract