AMMR1 Rabbit Polyclonal Antibody, 100ul Microbial Genome Editing and hereditary neuropathy with liability
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AMMR1 Rabbit Polyclonal Antibody, 100ul Microbial Genome Editing and hereditary neuropathy with liabilityThe exact function of this gene is not known, however, submicroscopic deletion of the X chromosome including this gene, COL4A5, and FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
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