The detail information of Motor neuron disease
OMIA Basic Information

Possible human homologues (MIM numbers):

Mendelian trait/disorder: unknown

Mode of inheritance: -

Considered a defect: yes

Year key mutation first reported: -

Species-specific name: -

Species-specific symbol: -

More detail information can see in

Associated Breeds
There are associated breeds.
Associated Gene
There are no associated genes.
References
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
2002 Rich,M.M.,Waldeck,R.F.,Cork,L.C.,Balice-Gordon,R.J.,Fyffe,R.E.W.,Wang,X.Y.,Cope,T.C.,Pinter,M.J.: :
Reduced endplate currents underlie motor unit dysfunction in canine motor neuron disease Journal of Neurophysiology 88:3293-3304, 2002.
Pubmed reference: 12466447 . DOI: 10.1152/jn.00270.2002 .
2002 Rich,M.M.,Wang,X.Y.,Cope,T.C.,Pinter,M.J.: :
Reduced neuromuscular quantal content with normal synaptic release time course and depression in canine motor neuron disease Journal of Neurophysiology 88:3305-3314, 2002.
Pubmed reference: 12466448 . DOI: 10.1152/jn.00271.2002 .
1999 Kent,M.,Knowles,K.,Glass,E.,deLahunta,A.,Braund,K.,Alroy,J.: :
Motor neuron abiotrophy in a Saluki Journal of the American Animal Hospital Association 35:436-439, 1999.
Pubmed reference: 10493421 .
1997 Pinter,M.J.,Waldeck,R.F.,Cope,T.C.,Cork,L.C.: :
Effects of 4-AMINOPYRIDINE on muscle and motor unit force in canine motor neuron disease Journal of Neuroscience 17:4500-4507, 1997.
Pubmed reference: 9151766 .