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. 2012 Oct 9;9:7–16. doi: 10.1007/8904_2012_174

Table 4.

Frequencies of the identified genotypes

Genotype # of patients
[N370S] + [W378C] 5
[G377S] + [G377S] 4
[V398I] + [V398I] 3
[N370S] + [I489T] 3
[R120W] + [N370S] 3
[793delC] + [N370S] 2
[N370S] + [L461P + IVS10+1G>T] 1
[Y313H] + [L444P] 1
[G377S] + [I489T] 1
[R353W] + [RecNciI] 1
[F213L] + [N370S] 1
[W179X] + [M361I + N370S] 1
[N188S] + [RecNciI] 1
[M123T] + [E349K] 1
[G377S] + [W378C] 1
[S125N] + [N370S] 1
[P245T] + [RecNciI] 1
[N396T] + [N396T] 1
[N370S] + [D399H] 1
[413delC] + [N370S] 1
[I489T] + [I489T] 1
[N370S] + [G377S] 1
[N396T] + [I489T] 1
[N396T] + [L444P] 1
[G202R] + [N370S] 1
[R131C] + [N370S] 1
[84insG] + [R496H] 1
[H311R] + [N370S] 1
[982-983insTGC] + [N370S] 1
[G377S] + [E326K + L444P] 1
[N370S] + [?] 3
[R48Q] + [?] 1
Total 48

? denotes unidentified mutation