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The chance of a mutation is unknown.
Correlation between the gross and histological subset of colorectal adenocarcinoma with KRAS mutation is unknown.
But the test misses mutations in about 20% of subjects whose familial mutation is unknown.
Whether this difference in growth is due to the laz1-4 mutatior or to a second site mutation is unknown.
Although the role of this mutation is unknown for human pathogenesis, it facilitates viral dissemination in Aedes albopictus mosquito that served as a vector for CHIKV during the recent Indian and the Indian Ocean area epidemics [30], [31].
One MDD subject carried essentially a homoplasmic mutation in DLPFC at ND4L T10652C, and two subjects with SZ showed less than 1% heteroplasmy; however, the pathological significance of the low levels of this non synonymous heteroplasmic mutation is unknown.
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Dr. Stedman, the lead researcher, said the cause of the mutation was unknown and probably unknowable: perhaps damage from cosmic rays, ingestion of toxins or other environmental exposures?
Despite the importance of Trak1 in health and disease, the mechanisms of Trak1 action remain unclear and the pathogenic effects of Trak1 mutation are unknown.
However, the molecular lesion causing the sctt mutation was unknown.
The effect on p53 function of this mutation was unknown.
In particular, the mechanisms for tissue specificity of the effects of VHL mutation are unknown.
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