Autosomal Dominant Juvenile Amyotrophic LS
DOI:
https://doi.org/10.15844/pedneurbriefs-13-9-9Keywords:
Amyotrophic Lateral Sclerosis, Sensory Conduction, Dorsal Root GangliaAbstract
The clinical and electrodiagnostic findings in 49 affected family members and neuropathological findings from two autopsies of a Maryland kindred with autosomal dominant juvenile amyotrophic lateral sclerosis (ALS) are reported from Johns Hopkins University and Hospital, Baltimore, MD.Published
1999-09-01
Issue
Section
Heredo-Degenerative Disorders
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Copyright (c) 1999 The Author(s)
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