Animal model of human disease. Motor neuron disease: Spinal muscular atrophy and amyotrophic lateral sclerosis

L. C. Cork; J. W. Griffin; R. J. Adams; D. L. Price

Animal model of human disease. Motor neuron disease: Spinal muscular atrophy and amyotrophic lateral sclerosis

L. C. Cork, J. W. Griffin, R. J. Adams, D. L. Price

School of Medicine

Research output: Contribution to journal › Article › peer-review

23 Scopus citations

Abstract

Hereditary canine spinal muscular atrophy (HCSMA) occurs in pure bred Brittany spaniels; the pattern of inheritance, clinical findings, electrodiagnostic studies, pathologic studies of muscle, and neuropathologic findings show features in common with human motor neuron disease.

Original language	English (US)
Pages (from-to)	599-602
Number of pages	4
Journal	American Journal of Pathology
Volume	100
Issue number	2
State	Published - Dec 1 1980

ASJC Scopus subject areas

Pathology and Forensic Medicine

Cite this

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title = "Animal model of human disease. Motor neuron disease: Spinal muscular atrophy and amyotrophic lateral sclerosis",

abstract = "Hereditary canine spinal muscular atrophy (HCSMA) occurs in pure bred Brittany spaniels; the pattern of inheritance, clinical findings, electrodiagnostic studies, pathologic studies of muscle, and neuropathologic findings show features in common with human motor neuron disease.",

author = "Cork, {L. C.} and Griffin, {J. W.} and Adams, {R. J.} and Price, {D. L.}",

year = "1980",

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AU - Cork, L. C.

AU - Griffin, J. W.

AU - Adams, R. J.

AU - Price, D. L.

PY - 1980/12/1

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N2 - Hereditary canine spinal muscular atrophy (HCSMA) occurs in pure bred Brittany spaniels; the pattern of inheritance, clinical findings, electrodiagnostic studies, pathologic studies of muscle, and neuropathologic findings show features in common with human motor neuron disease.

AB - Hereditary canine spinal muscular atrophy (HCSMA) occurs in pure bred Brittany spaniels; the pattern of inheritance, clinical findings, electrodiagnostic studies, pathologic studies of muscle, and neuropathologic findings show features in common with human motor neuron disease.

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Animal model of human disease. Motor neuron disease: Spinal muscular atrophy and amyotrophic lateral sclerosis

Abstract

ASJC Scopus subject areas

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