Neurofibromin Polyclonal Antibody, 50ul Glassware Sets cause factor IX deficiency

cause factor IX deficiency

This locus encodes both the light and heavy subunits of acyloxyacyl hydrolase

The expression pattern of a similar rat protein suggests that this protein may be involved in neurovascular function in the brain

It is also expressed in embryonic and adult olfactory neuroepithelia where it complexes with eukaryotic translation initiation factor 4E (eIF4E) and possibly regulates mRNA transport or translation

autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13)

Neurofibromin Polyclonal Antibody, 50ul Glassware Sets cause factor IX deficiencyNF1 product appears to function as a negative regulator of the ras signal transduction pathway. Mutations in this gene have been linked to neurofibromatosis type 1, juvenile myelomonocytic leukemia and Watson syndrome. The mRNA for this gene is subject to RNA editing (CGA>UGA >Arg1306Term) resulting in premature translation termination. Alternatively spliced transcript variants encoding different isoforms have also been described for this gene.