La neuropathie sensitivo-motrice héréditaire avec agénésie du corps calleux

Heidi C. Howard; Nicolas Dupré; Jean Mathieu; Jean-Pierre Bouchard; Guy A. Rouleau

doi:10.1051/medsci/2003194414

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Volume 19 / No 4 (Avril 2003)

Med Sci (Paris), 19 4 (2003) 414-416

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Issue		Med Sci (Paris) Volume 19, Number 4, Avril 2003


Page(s)		414 - 416
Section		Le Magazine : Nouvelles
DOI		https://doi.org/10.1051/medsci/2003194414
Published online		15 April 2003

De Braekeleer M, Dallaire A, Mathieu J. Genetic epidemiology of sensorimotor polyneuropathy with or without agenesis of the corpus callosum in northeastern Quebec. Hum Genet 1993; 91: 223–7. [Google Scholar]
Howard H, Mount DB, Rochefort D, et al. The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum. Nat Genet 2002; 32: 384–92. [Google Scholar]
Mathieu J, Bédard F, Prévost C, Langevin P. Neuropathie sensitivomotrice héréditaire avec ou sans agénésie du corps calleux: étude radiologique et clinique de 64 cas. Can J Neurol Sci 1990; 17: 103–8. [Google Scholar]
Carpenter S. The pathology of the Andermann syndrome. In: Lassonde M, Jeeves M, eds. Callosal agenesis: a natural split brain? New York: Plenum Press, 1994 : 27–30. [Google Scholar]
Hiki K, D’Andrea R, Furze J, et al. Cloning, characterization, and chromosomal location of a novel human K-Cl cotransporter. J Biol Chem 1999; 274: 10661–7. [Google Scholar]
Dobyns W. Absence makes the search grow longer. Am J Hum Genet 1996; 58: 7–16. [Google Scholar]
Mahadevan A, Santosh V, Gayatri N, et al. Infantile neuroaxonal dystrophy and giant axonal neuropathy: overlap diseases of neuronal cytoskeletal elements in childhood? Clin Neuropathol 2000; 19: 221–9. [Google Scholar]

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[1] De Braekeleer M, Dallaire A, Mathieu J. Genetic epidemiology of sensorimotor polyneuropathy with or without agenesis of the corpus callosum in northeastern Quebec. Hum Genet 1993; 91: 223–7. [Google Scholar]

[2] Howard H, Mount DB, Rochefort D, et al. The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum. Nat Genet 2002; 32: 384–92. [Google Scholar]

[3] Mathieu J, Bédard F, Prévost C, Langevin P. Neuropathie sensitivomotrice héréditaire avec ou sans agénésie du corps calleux: étude radiologique et clinique de 64 cas. Can J Neurol Sci 1990; 17: 103–8. [Google Scholar]

[4] Carpenter S. The pathology of the Andermann syndrome. In: Lassonde M, Jeeves M, eds. Callosal agenesis: a natural split brain? New York: Plenum Press, 1994 : 27–30. [Google Scholar]

[5] Hiki K, D’Andrea R, Furze J, et al. Cloning, characterization, and chromosomal location of a novel human K-Cl cotransporter. J Biol Chem 1999; 274: 10661–7. [Google Scholar]

[6] Dobyns W. Absence makes the search grow longer. Am J Hum Genet 1996; 58: 7–16. [Google Scholar]

[7] Mahadevan A, Santosh V, Gayatri N, et al. Infantile neuroaxonal dystrophy and giant axonal neuropathy: overlap diseases of neuronal cytoskeletal elements in childhood? Clin Neuropathol 2000; 19: 221–9. [Google Scholar]