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Family with sequence similarity 13, member C is a protein that in humans is encoded by the FAM13C gene.[5]
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000148541 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000043259 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: Family with sequence similarity 13, member C".
Further reading
- Wu JH, Lemaitre RN, Manichaikul A, Guan W, Tanaka T, Foy M, Kabagambe EK, Djousse L, Siscovick D, Fretts AM, Johnson C, King IB, Psaty BM, McKnight B, Rich SS, Chen YD, Nettleton JA, Tang W, Bandinelli S, Jacobs DR, Browning BL, Laurie CC, Gu X, Tsai MY, Steffen LM, Ferrucci L, Fornage M, Mozaffarian D (April 2013). "Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium". Circulation: Cardiovascular Genetics. 6 (2): 171–83. doi:10.1161/CIRCGENETICS.112.964619. PMC 3891054. PMID 23362303.
- Karasik D, Hsu YH, Zhou Y, Cupples LA, Kiel DP, Demissie S (July 2010). "Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study". Journal of Bone and Mineral Research. 25 (7): 1555–63. doi:10.1002/jbmr.38. PMC 3153998. PMID 20200953.
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