AFG3L2 Polyclonal Antibody, 100ul Drug Development and Evaluation severe brain atrophy

severe brain atrophy

This gene encodes a member of the cGMP-inhibited cyclic nucleotide phosphodiesterase (cGI-PDE) family

There are two pseudogenes for RPS6KB1 on chromosome 17

GSC2 is expressed in a limited number of adult tissues

The centromeric copy may be a modifier of disease caused by mutation in the telomeric copy

AFG3L2 Polyclonal Antibody, 100ul Drug Development and Evaluation severe brain atrophyThis gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.