Spinal and bulbar muscular atrophy is a debilitating neurodegenerative disorder caused by degeneration of motor neurons in the brainstem and spinal cord, and muscle wasting.
The condition is associated with a mutation of the androgen receptor (AR) gene.
Axol’s cell line derived from a Spinal and bulbar muscular atrophy patient is an excellent model for investigating this rare inherited disease.
Explore a library of lines, including Spinal and Bulbar Muscular Atrophy donors for custom manufacturing projects
| Donor Condition | Lines Available |
| Spinal and bulbar muscular atrophy (SBMA) | Male, 66, AR: >47 CAG |
