PUBLICATION

CORRECTION: Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy

Authors
Yuen, M., Sandaradura, S.A., Dowling, J.J., Kostyukova, A.S., Moroz, N., Quinlan, K.G., Lehtokari, V.L., Ravenscroft, G., Todd, E.J., Ceyhan-Birsoy, O., Gokhin, D.S., Maluenda, J., Lek, M., Nolent, F., Pappas, C.T., Novak, S.M., D'Amico, A., Malfatti, E., Thomas, B.P., Gabriel, S.B., Gupta, N., Daly, M.J., Ilkovski, B., Houweling, P.J., Davidson, A.E., Swanson, L.C., Brownstein, C.A., Gupta, V.A., Medne, L., Shannon, P., Martin, N., Bick, D.P., Flisberg, A., Holmberg, E., Van den Bergh, P., Lapunzina, P., Waddell, L.B., Sloboda, D.D., Bertini, E., Chitayat, D., Telfer, W.R., Laquerrière, A., Gregorio, C.C., Ottenheijm, C.A., Bönnemann, C.G., Pelin, K., Beggs, A.H., Hayashi, Y.K., Romero, N.B., Laing, N.G., Nishino, I., Wallgren-Pettersson, C., Melki, J., Fowler, V.M., MacArthur, D.G., North, K.N., Clarke, N.F.
ID
ZDB-PUB-220906-10
Date
2015
Source
The Journal of Clinical Investigation   125: 456-7 (Other)
Registered Authors
Keywords
none
MeSH Terms
none
PubMed
25654555 Full text @ Journal of Clin. Invest.
Abstract
In the original version of the article, the mutation c.601_602delGA in LMOD3 was incorrectly described; the correct predicted protein change is p.D201Qfs*9. In addition, the LMOD3 mutation p.S47Qfs*13 was incorrectly indicated; the correct mutation is S47Qfs*13. These errors affected portions of Table 1, Table 2, Figure 1, and Supplemental Table 2. The corrected versions of Table 1, Table 2, and Figure 1 appear below, and Supplemental Table 2 has been updated online.
Errata / Notes
This article corrects ZDB-PUB-140925-3.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping