In the original article, there was a mistake in Table 1 as published. For patients 16 and 17, the protein alteration resulting from the c. 107545delG mutation should be p.Ala35849Glnfs*16. The corrected Table 1 appears below.
Table 1
| Patient no. | Gene | Chromosome | Exon | Transcript no. | Nucleotide | Protein | Reference |
|---|---|---|---|---|---|---|---|
| 1 | DES | 2 | 7 | NM_1927 | c.1256C>T | p.Pro419Leu | None |
| 2 | DES | 2 | 7 | NM_1927 | c.1256C>T | p.Pro419Leu | None |
| 3 | DES | 2 | 7 | NM_1927 | c.1256C>T | p.Pro419Leu | None |
| 4 | DES | 2 | 7 | NM_1927 | c.1256C>T | p.Pro419Leu | None |
| 5 | DES | 2 | 6 | NM_1927 | c.1096_1098delACA | p.Asn366del | (14) |
| 6 | DES | 2 | 6 | NM_1927 | c.1096_1098delACA | p.Asn366del | (14) |
| 7 | DES | 2 | 6 | NM_1927 | c.1096_1098delACA | p.Asn366del | (14) |
| 8 | DES | 2 | 6 | NM_1927 | c.1076_1077ins GGCCAGTGG | p.Glu359delins GluAlaSerGly | None |
| 9 | BAG3 | 10 | 3 | NM_004281 | c.626C>T | p.Pro209Leu | (15) |
| 10 | BAG3 | 10 | 3 | NM_004281 | c.626C>T | p.Pro209Leu | (15) |
| 11 | FLNC | 7 | 36 | NM_001458 | c.6004+3G>A | splicing | None |
| 12 | FLNC | 7 | 33 | NM_001458 | c.5468C>T | P.Thr1823Met | None |
| 13 | FHL1 | X | 5 | NM_001159702 | c.386G>A | p.Cys129Tyr | None |
| 14 | TTN | 2 | 344 | NM_001267550 | c.95134T>C | p.Cys31712Arg | (16–22) |
| 15 | TTN | 2 | 344 | NM_001267550 | c.95185T>C | p.Trp31729Arg | (23) |
| 16 | TTN | 2 | 69 | NM_001267550 | c. 19993G>T | p.Glu6665X | None |
| 363 | NM_001267550 | c. 107545delG | p.Ala35849Glnfs*16 | None | |||
| 17 | TTN | 2 | 69 | NM_001267550 | c. 19993G>T | p.Glu6665X | None |
| 363 | NM_001267550 | c. 107545delG | p.Ala35849Glnfs*16 | None | |||
| 18 | None | - | - | - | - | - | - |
Genetics of the present MFM patient cohort.
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
Summary
Keywords
myofibrillar myopathy, desminopathy, titinopathy, BAG3opathy, filaminopathy, FHL1opathy
Citation
Luo Y-B, Peng Y, Lu Y, Li Q, Duan H, Bi F and Yang H (2021) Corrigendum: Expanding the Clinico-Genetic Spectrum of Myofibrillar Myopathy: Experience From a Chinese Neuromuscular Center. Front. Neurol. 11:636981. doi: 10.3389/fneur.2020.636981
Received
02 December 2020
Accepted
03 December 2020
Published
08 January 2021
Approved by
Frontiers Editorial Office, Frontiers Media SA, Switzerland
Volume
11 - 2020
Updates
Copyright
© 2021 Luo, Peng, Lu, Li, Duan, Bi and Yang.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Huan Yang yangh69@126.com
This article was submitted to Neuromuscular Diseases, a section of the journal Frontiers in Neurology
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