CNBP
Template:PBB Cellular nucleic acid-binding protein is a protein that in humans is encoded by the CNBP gene.[1][2][3]
External links
- GeneReviews/NCBI/NIH/UW entry on Myotonic Dystrophy Type 2
- ZNF9+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
References
- ^ Lusis AJ, Rajavashisth TB, Klisak I, Heinzmann C, Mohandas T, Sparkes RS (1991). "Mapping of the gene for CNBP, a finger protein, to human chromosome 3q13.3-q24". Genomics. 8 (2): 411–4. doi:10.1016/0888-7543(90)90303-C. PMID 2249857.
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ignored (help)CS1 maint: multiple names: authors list (link) - ^ Liquori CL, Ricker K, Moseley ML, Jacobsen JF, Kress W, Naylor SL, Day JW, Ranum LP (2001). "Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9". Science. 293 (5531): 864–7. doi:10.1126/science.1062125. PMID 11486088.
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ignored (help)CS1 maint: multiple names: authors list (link) - ^ "Entrez Gene: CNBP CCHC-type zinc finger, nucleic acid binding protein".
Rajavashisth TB, Taylor AK, Andalibi A, et al. (1989). "Identification of a zinc finger protein that binds to the sterol regulatory element.". Science 245 (4918): 640–3. doi:10.1126/science.2562787. PMID 2562787.
Further reading
Rajavashisth TB, Taylor AK, Andalibi A, et al. (1989). "Identification of a zinc finger protein that binds to the sterol regulatory element.". Science 245 (4918): 640–3. doi:10.1126/science.2562787. PMID 2562787.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.