Quantitation of Meissner's corpuscles in hereditary neurologic disorders: Charcot-Marie-Tooth disease, Roussy-Levy syndrome, Dejerine-Sottas disease, hereditary sensory neuropathy, spinocerebellar degenerations, and hereditary spastic paraplegia (Q72874793)
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scientific article published on 01 January 1966
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Quantitation of Meissner's corpuscles in hereditary neurologic disorders: Charcot-Marie-Tooth disease, Roussy-Levy syndrome, Dejerine-Sottas disease, hereditary sensory neuropathy, spinocerebellar degenerations, and hereditary spastic paraplegia |
scientific article published on 01 January 1966 |
Statements
Quantitation of Meissner's corpuscles in hereditary neurologic disorders. Charcot-Marie-Tooth disease, Roussy-Levy syndrome, Dejerine-Sottas disease, hereditary sensory neuropathy, spinocerebellar degenerations, and hereditary spastic paraplegia (English)
Quantitation of Meissner's corpuscles in hereditary neurologic disorders: Charcot-Marie-Tooth disease, Roussy-Levy syndrome, Dejerine-Sottas disease, hereditary sensory neuropathy, spinocerebellar degenerations, and hereditary spastic paraplegia (English)
1 reference
P. J. Dyck
R. K. Winkelmann