Human Molecular Genetics 2006 15(1):163-165; doi:10.1093/hmg/ddi437
© The Author 2005. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org
Polymorphisms in the FCN2 gene determine serum variation and function of Ficolin-2
T. Hummelshoj,
L. Munthe-Fog,
H.O. Madsen,
T. Fujita,
M. Matsushita and
P. Garred
Human Molecular Genetics (2005) 14, 16511658; doi:10.1093/hmg/ddi173
The authors would like to apologize for the following errors that appeared in the above article. Tables 1 and 3 are reprinted in their entirely.
Results, section FCN1, exon 1, 6 and 8
is changed to exon 1, 7 and 9 on page 1652, line
4 in the Resultry section.
Table 1. FCN1 mutations, row 11, exon 6 is changed to exon 7
| FCN1+5358C>T |
rs2274845 |
Exon 7 |
|
60 |
24 (40.0) |
28 (46.7) |
8 (13.3) |
0.367 |
|
Table 1. FCN1 mutations, row 12, exon 8 is changed to exon 9
| FCN1+7918G>A |
rs1071583 |
Exon 9 |
|
60 |
24 (40.0) |
28 (46.7) |
8 (13.3) |
0.367 |
|
Table 1. FCN2 mutations, row 11, 5048T>C, ss32469543, 23 (38.3), 28 (46.7), 9 (15.0), 0.383 is changed to 5060C>T, ss48532605, 56 (93.3), 4 (6.7), 0 (0.0), 0.967
| FCN2+5060C>T |
ss48532605 |
Exon 6 |
|
60 |
56 (93.3) |
4 (6.7) |
0 (0.0) |
0.967 |
|
Table 3. FCN2, line 10, tgtgggacgtcggcctgg is changed to caggtgggcgtgctggtg ttgcagatggcccaggcc is changed to cagcccaggcccaagagg
| Exon 6 |
5'-caggtgggcgtgctggtg-3' |
5'-cagcccaggcccaagagg-3' |
|

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