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Ile408Val mutation is located in the cytoplasmatic tail.
This mutation is located in a splice lariat branch point sequence.
Preliminary data from our ongoing gene-mapping work suggest that the LSE3 mutation is located in a single locus (data not shown).
The "white" mutation is located on the X chromosome and results in lack of pigment, poor eyesight, and lower fitness (Jones and Probert 1980; Reed and Reed 1950).
This mutation is located in S4-transmembrane segments of a protein domain II, which is considered the channel voltage sensor segment.
The mutation is located on a part of the protein that normally binds with the LDL receptor, and binding is reduced as a result of the mutation.
The G1485A mutation is located in an intron encoding splice site.
The third mutation is located in a different exon with distal spacing.
The p.Arg423His mutation is located in the highly conserved S4 domain of the channel.
This mutation is located in the linker region between domain 3b and 2 and is structurally adjacent to Glu379.
In fact, this intron mutation is located 180 bp downstream from exon 3 and potentially modifies splicing events (Figure 2A).
More suggestions(15)
mutant is located
mutation is linked
mutation is labeled
mutation is parametrised
mutation is known
mutation is shown
mutation is implemented
mutation is considered
mutation is required
mutation is done
mutation is identified
mutation is inherited
mutation is presented
mutation is determined
mutation is generated
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