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  5. Neuropathy- congenital- with arthrogryposis...

Neuropathy- congenital- with arthrogryposis multiplex

December 31, 2014

Latest Research

  • <em>CNTNAP1</em> Mutations and Their Clinical Presentations: New Case Report and Systematic Review
  • A case of congenital spinal muscular atrophy with pain due to a mutation in TRPV4
  • A distinct congenital motor and sensory neuropathy (neuronal type) with dysmorphic features in a father and two sons. A variant of Charcot-Marie-Tooth disease
  • A new form of congenital proprioceptive sensory neuropathy associated with arthrogryposis multiplex
  • Absence of Axoglial Paranodal Junctions in a Child With CNTNAP1 Mutations, Hypomyelination, and Arthrogryposis
More Research
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