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The Q141K mutation is also linked with this phenotype of renal uric acid overload, both in patients who are homozygous for Q141K and those who are heterozygous for Q126X and Q141K

Both are more closely related to gliadins than the other protein types discussed below, but lack the repeated sequences which are typical of gliadins

Sleep Med Rev 17(3):21525 Laskemoen JF et al (2019) Sleep disturbances in schizophrenia spectrum and bipolar disorders a transdiagnostic perspective

Breast cancer treatment outcome with adjuvant tamoxifen relative to patient CYP2D6 and CYP2C19 genotypes

As a result, anti-doping testing panels are specifically designed to identify these peptides even if routine drug tests cannot