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This guide covers every facet of the documentation and coding encounter, from CDI query triggers and GLP-1 medication coding to HCC v28 mapping and complication sequencing
2024 Jan 14;131(1):92-102
Two of these SNPs, rs2274223 and rs3765524 result in missense mutations in the coding region of PLCE1 gene and cause the amino acid substitutions His1927Arg in the C2 domain and Thr1777Ile in the catalytic domain, respectively [28]
Endocrinology 158 , 42184232 (2017)
Spiegel R, Kalla R, Mantokoudis G, Maire R, Mueller H, Hoerr R, Ihl R
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