Variation in SIPA1L2 is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A

Overview of attention for article published in Annals of Neurology, February 2019

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RT @doctorappletini: #neurology #neuromuscular #neuropathy #cmt https://t.co/EO73U4cjkH

#neurology #neuromuscular #neuropathy #cmt

RT @HIHGatUM: The key to developing new treatments for Charcot-Marie-Tooth disease type 1A could be the modification of a gene called SIPA1…

The key to developing new treatments for Charcot-Marie-Tooth disease type 1A could be the modification of a gene called SIPA1L2, suggests a study by HIHG researchers https://t.co/2wcQqIZzIp https://t.co/ODke1Yb3Qz

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