CYTSA Rabbit Polyclonal Antibody, 100ul Bottles Mutations in SLC52A2 have been

Mutations in SLC52A2 have been associated with Brown-Vialetto-Van Laere syndrome 2--an autosomal recessive progressive neurologic disorder characterized by deafness

making it ideal for Cell Culture Applications

The dysregulation of the signaling pathways mediated by this protein may be the cause of the APLL

and shal - have been identified in Drosophila

CDKL3 was identified as a gene absent in leukemic patients with chromosome 5q deletion

CYTSA Rabbit Polyclonal Antibody, 100ul Bottles Mutations in SLC52A2 have beenThis gene encodes a coiled coil domain containing protein. The encoded protein may play a critical role in actin cytoskeletal reorganization during facial morphogenesis. Mutations in this gene are a cause of oblique facial clefting 1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. A read through transcript composed of SPECC1L (sperm antigen with calponin homology and coiled coil domains 1 like)