Identification of a rare SEPT9 variant in a family with autosomal dominant Charcot-Marie-Tooth disease

Overview of attention for article published in BMC Medical Genomics, March 2020

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RT @werner_hauke: First report of a #CMT #neuropathy family with a mutated #septin gene, a rare variant affecting the GTP binding domain of…

RT @werner_hauke: First report of a #CMT #neuropathy family with a mutated #septin gene, a rare variant affecting the GTP binding domain of…

First report of a #CMT #neuropathy family with a mutated #septin gene, a rare variant affecting the GTP binding domain of #SEPT9 https://t.co/mZo45OP4pS

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