Mesh term Bulbo-Spinal Atrophy, X-Linked
Browse to parent terms:Genetic Diseases, X-Linked
Heredodegenerative Disorders, Nervous System
Muscular Atrophy, Spinal
Description
An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR.Search for this term in our Faculty Database
View this term at the NCBI website
