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Anani T, Sindou P, Richard L, et al. Ultrastructural Immunocytochemical Abnormalities of Peripheral Myelin Proteins in Hereditary Sensory-Motor Neuropathies: 12 cases. Ann N Y Acad Sci. 1999;883(1):186-195doi: 10.1111/j.1749-6632.1999.tb08581.x.
Anani, T., Sindou, P., Richard, L., Diot, M., & Vallat, J. M. (1999). Ultrastructural Immunocytochemical Abnormalities of Peripheral Myelin Proteins in Hereditary Sensory-Motor Neuropathies: 12 cases. Annals of the New York Academy of Sciences, 883(1), 186-195. https://doi.org/10.1111/j.1749-6632.1999.tb08581.x
Anani, Thierry, et al. "Ultrastructural Immunocytochemical Abnormalities of Peripheral Myelin Proteins in Hereditary Sensory-Motor Neuropathies: 12 cases." Annals of the New York Academy of Sciences vol. 883,1 (1999): 186-195. doi: https://doi.org/10.1111/j.1749-6632.1999.tb08581.x
Anani T, Sindou P, Richard L, Diot M, Vallat JM. Ultrastructural Immunocytochemical Abnormalities of Peripheral Myelin Proteins in Hereditary Sensory-Motor Neuropathies: 12 cases. Ann N Y Acad Sci. 1999 Oct;883(1):186-195. doi: 10.1111/j.1749-6632.1999.tb08581.x. PMID: 29086953.
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Ann N Y Acad Sci. 1999 Oct;883(1):186-195. doi: 10.1111/j.1749-6632.1999.tb08581.x.

Ultrastructural Immunocytochemical Abnormalities of Peripheral Myelin Proteins in Hereditary Sensory-Motor Neuropathies: 12 cases.

Annals of the New York Academy of Sciences

Thierry Anani, Philippe Sindou, Laurence Richard, Martine Diot, Jean-Michel Vallat

Affiliations

  1. Department of Neurology, University Hospital, 2 Avenue Martin Luther King, 87402 Limoges, France.

PMID: 29086953 DOI: 10.1111/j.1749-6632.1999.tb08581.x

Abstract

Hereditary sensorimotor neuropathies form a heterogeneous group of genetically determined diseases, of which Charcot-Marie-Tooth (CMT) disease is the most common. In order to establish relations between genotype and the expression of peripheral myelin proteins, we carried out a quantitative study by ultrastructural immunocytochemistry of several myelin proteins (PMP22, P

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