EphA1 Monoclonal Antibody, 100ul Bottle-Top Dispenser Mutations in this gene cause

Mutations in this gene cause speech-language disorder 1 (SPCH1)

which contains no introns in either its coding or untranslated sequences

In Burkitt's lymphoma cell lines

A truncated version representing a pseudogene (RDXP2) was assigned to Xp21

the exchanger may play a key role in digitalis action

EphA1 Monoclonal Antibody, 100ul Bottle-Top Dispenser Mutations in this gene causeThis gene belongs to the ephrin receptor subfamily of the protein tyrosine kinase family. EPH and EPH related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their