Autosomal dominant GDAP1 mutation with severe phenotype and respiratory involvement: A case report

Overview of attention for article published in Frontiers in Neurology, October 2022

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RT @FrontNeurol: New Research: Autosomal dominant GDAP1 mutation with severe phenotype and respiratory involvement: A case report: Charcot…

27 Oct 2022

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Autosomal dominant GDAP1 mutation with severe phenotype and respiratory involvement: A case report: Charcot Marie Tooth (CMT) is a heterogeneous group of genetic disorders characterized by progressive motor and sensory… #Neurology https://t.co/M6hzDBhO1y

25 Oct 2022

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New Research: Autosomal dominant GDAP1 mutation with severe phenotype and respiratory involvement: A case report: Charcot Marie Tooth (CMT) is a heterogeneous group of genetic disorders characterized by progressive motor and sensory… https://t.co/yIYmBPoAO

24 Oct 2022

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