OR2W3

OR2W3

in gene, was identified as a potentially causative mutation for autosomal dominant RP. The mutation co-segregated with the.
Complete information for gene (Protein Coding), Olfactory Receptor Family 2 Subfamily W Member 3, including: function, proteins, disorders, pathways.
olfactory receptor family 2 subfamily W member 3 [ (human)]. Gene ID: updated on.
OR2W3 CAS PubMed Article Colbert, H. Retrieved from " wikigadugi.org? ISI CAS PubMed Article Cordle, J. RefSeqs OR2W3 chromosomes and scaffolds contigs from both reference and alternate. Send me a copy of this email. Bracket - Mama Africa (Dance Video) #AzontoBradez