The presence of the Glu318Gly mutation was associated with significantly lower cognitive performance when compared to controls (P = 0.011).
The C282Y mutation was associated with nonsignificantly increased risk of CHD (relative risk=1.60, 95% CI 0.9 2.9).
The researchers next looked at whether this same mutation was associated with FSF susceptibility, comparing 28 affected and 16 healthy Shar-Peis.
Each single mutation was associated with a distinct microsatellite haplotype.
The G357S mutation was associated with the A370T mutation (q-value = 2.93E−13).
Here, the decrease in frequency of this mutation was associated with treatment (Figures 2 and 3).
The mutation was associated with late fetal death and stillbirth in at least 42.6% of the offspring of YN51.
This mutation was associated with lack of function in vitro; moreover, it was associated with drug resistance in vivo.
The dense nuclear cataract caused by the γB-crystallin S11R mutation was associated with the deterioration of intracellular components in fiber cells of the lens core (Figure 2).
The W680R mutation was associated with an N at position 677, a Q at position 683, and an L at position 686.
The W680G mutation was associated with a K at position 677, a Q at position 683, and an I at position 686.
