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Although the gene involved has been identified, there is no screening test for Marfan's, because so many different mutations can be responsible for the syndrome.
Mutations can be beneficial, but they are much more likely to be harmful — which means the changes will be overwhelmingly negative.
The mutations can be inherited from the parents or they can arise spontaneously in the fetus.
Null alleles or mutations can be treated.
0.424 Mutations can be passed down to the next generation.
Gene mutations can be induced by radiation as a result of chromosomal translocations.
(A complete list of all mutations can be found in Table S1).
The additional risk of thrombosis during pregnancy associated with such genetic mutations can be substantial.
The acquired genomic mutations can be generic or membrane protein specific.
Mutations can be detected in 90%.
The Q61R and Q61L NRAS mutations can be detected by targeted sequencing.
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