Familial myoclonus, cerebellar ataxia, and deafness. Specific genetically-determined disease.
May, D L
Familial myoclonus, cerebellar ataxia, and deafness. Specific genetically-determined disease. [electronic resource] - Archives of neurology Sep 1968 - 331-8 p. digital
Publication Type: Journal Article
0003-9942
10.1001/archneur.1968.00480030109013 doi
Adult
Aged
Cerebellar Ataxia--genetics
Cerebral Cortex--physiopathology
Deafness--genetics
Electroencephalography
Female
Humans
Light
Male
Middle Aged
Muscles--physiopathology
Myoclonus--classification
Pedigree
Familial myoclonus, cerebellar ataxia, and deafness. Specific genetically-determined disease. [electronic resource] - Archives of neurology Sep 1968 - 331-8 p. digital
Publication Type: Journal Article
0003-9942
10.1001/archneur.1968.00480030109013 doi
Adult
Aged
Cerebellar Ataxia--genetics
Cerebral Cortex--physiopathology
Deafness--genetics
Electroencephalography
Female
Humans
Light
Male
Middle Aged
Muscles--physiopathology
Myoclonus--classification
Pedigree