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De novo mutation of the myelin Po gene in Dejerine–Sottas disease (hereditary motor and sensory neuropathy type III)
National licenceNature Publishing Group | 1993| -
A Novel Homozygous Mutation of the Myelin Po Gene Producing Dejerine-Sottas Disease (Hereditary Motor and Sensory Neuropathy Type III)
Online Contents | 1996|Contributors: Ouvrier, Robert -
Mutations in the gene encoding immunoglobulin μ-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1
National licenceNature Publishing Group | 2001|
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