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Amyotrophic lateral sclerosis 8: ALS8. A form of amyotrophic lateral sclerosis (ALS) inherited in an autosomal dominant manner due to mutation in a gene on chromosome 20ptel.
Amyotrophic lateral sclerosis 8 information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
Amyotrophic lateral sclerosis, or ALS, is a disease of the nerve cells in the brain and ... Review Date: 8/27/2010. Reviewed by: David C. Dugdale, III, MD ...
The Amyotrophic Lateral Sclerosis 8 protein VAPB is cleaved, secreted, and acts as a ligand for Eph receptors
Researchers have identified genetic mutations that cause amyotrophic lateral sclerosis types 1, 2, 4, and 8. Onset of symptoms in adulthood is characteristic ...
Amyotrophic lateral sclerosis, familial type 8 information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention ...