Absence of Axoglial Paranodal Junctions in a Child With CNTNAP1 Mutations, Hypomyelination, and Arthrogryposis

Overview of attention for article published in Journal of Child Neurology, June 2018

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A leukodystrophy with absence of axoglial septate paranodal junctions: https://t.co/ATZ4ME5DjX @ChildrensPhila @childrensnation https://t.co/tMOZfsseHM

07 Sep 2018

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RT @JChildNeurol: Online first: Arthrogryposis multiplex congenita from genetic leukodystrophy along with severe progressive peripheral dem…

08 Jul 2018

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Online first: Arthrogryposis multiplex congenita from genetic leukodystrophy along with severe progressive peripheral demyelinating neuropathy from the absence of septate paranodal junctions: https://t.co/ATZ4ME5DjX @childrenshealth @genome_gov @GWSMHS @MC

19 Jun 2018

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CNTNAP1 #mutations https://t.co/avK3piw7iS leading to absence of axoglial paranodal junctions in a child with #hypomyelination, and #arthrogryposis https://t.co/0C3L2QCFVV

19 Jun 2018

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