Biology:FAM13C
From HandWiki
Short description: Protein-coding gene in the species Homo sapiens
Generic protein structure example |
Family with sequence similarity 13, member C is a protein that in humans is encoded by the FAM13C gene.[1]
References
Further reading
- "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. April 2013. doi:10.1161/CIRCGENETICS.112.964619. PMID 23362303.
- "Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study". Journal of Bone and Mineral Research 25 (7): 1555–63. July 2010. doi:10.1002/jbmr.38. PMID 20200953.
Original source: https://en.wikipedia.org/wiki/FAM13C.
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