Biology:SLC35F1
From HandWiki
Short description: Protein-coding gene in the species Homo sapiens
Solute carrier family 35, member F1 is a protein that in humans is encoded by the SLC35F1 gene.[1] The gene is also known as C6orf169 or dJ230I3.1.[1]
References
Further reading
- Sotoodehnia, N.; Isaacs, A.; De Bakker, P. I. W.; Dörr, M.; Newton-Cheh, C.; Nolte, I. M.; Van Der Harst, P.; Müller, M. et al. (2010). "Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction". Nature Genetics 42 (12): 1068–1076. doi:10.1038/ng.716. PMID 21076409.
- Eijgelsheim, M.; Newton-Cheh, C.; Sotoodehnia, N.; De Bakker, P. I. W.; Müller, M.; Morrison, A. C.; Smith, A. V.; Isaacs, A. et al. (2010). "Genome-wide association analysis identifies multiple loci related to resting heart rate". Human Molecular Genetics 19 (19): 3885–3894. doi:10.1093/hmg/ddq303. PMID 20639392.
 |  |
