Clinical spectrum of Transthyretin amyloidogenic mutations among diverse population origins.

In our phenome-wide analysis, we identified a total of 179 nominally significant associations ( p < 0.05; Fig. 1 , Supplemental Table 5 ) with respect to TTR Ala81Thr, His90Asn, and Val122Ile mutations (60, 54, and 65 associations, respectively).

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