C9orf72-associated SMCR8 protein binds in the ubiquitin pathway and with proteins linked with neurological disease
A pathogenic GGGCCC hexanucleotide expansion in the first intron/promoter region of the C9orf72 gene is the most common mutation associated with amyotrophic lateral sclerosis (ALS). The C9orf72 gene product forms...
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Acta Neuropathologica Communications 2020
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