Novel homozygous missense mutation in GAN associated with Charcot-Marie-Tooth disease type 2 in a large consanguineous family from Israel

Overview of attention for article published in BMC Medical Genomics, November 2016

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RT @BPNSociety: Missense mutation n GAN associated with CMT2 https://t.co/Kx3szzRcAX

Missense mutation n GAN associated with CMT2 https://t.co/Kx3szzRcAX

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