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Erschienen in: BMC Medical Genetics 1/2019

Open Access 01.12.2019 | Correction

Correction to: Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10

verfasst von: Amjad Khan, Rongrong Wang, Shirui Han, Muhammad Umair, Safdar Abbas, Muhammad Ismail Khan, Mohammad A. Alshabeeb, Majid Alfadheland, Xue Zhang

Erschienen in: BMC Medical Genetics | Ausgabe 1/2019

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Amjad Khan and Rongrong Wang contributed equally to this work.
The original article can be found online at https://​doi.​org/​10.​1186/​s12881-019-0895-7
Correction to: BMC Med Genet (2019) 20:166
https://doi.org/10.1186/s12881-019-0895-7
Please be advised that following publication of the original article [1], the authors have identified the following errors with the scientific content:
Fig. 1 (please note that the corrected Fig. 1 is enclosed in this article):
In part ‘(E)’, the arrow which indicates the location of the p. Arg32936His variant is incorrectly positioned
In part ‘(F)’, the amino acids should be in the N–C orientation, with the “O” letters replaced by “D”s
Legend of Fig. 1 (specifically, in the part concerning ‘1e’):
“(The novel missense variant p. Arg32936His reported here is indicated in red localized in the M domain)” should instead read “(The novel missense variant p. Arg32936His reported here is indicated in red localized in the FN3 domain 128, which is situated in the distal A-band region)”
In subsection (of the ‘Results’ section) ‘Whole genome sequencing’:
“the amino acid (aa) sequence located in the M domain of TTN gene” should instead read “the amino acid (aa) sequence located in the FN3 domain 128 of TTN gene”
In the ‘Discussion’ section:
“Carriage of the mutation c.98807G > A which is very close to the M domain of the TTN gene” should instead read “Carriage of the mutation c.98807G > A which is in the FN3 domain 128 of TTN gene”
The authors apologize for this error.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
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Titel
Correction to: Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10
verfasst von
Amjad Khan
Rongrong Wang
Shirui Han
Muhammad Umair
Safdar Abbas
Muhammad Ismail Khan
Mohammad A. Alshabeeb
Majid Alfadheland
Xue Zhang
Publikationsdatum
01.12.2019
Verlag
BioMed Central
Erschienen in
BMC Medical Genetics / Ausgabe 1/2019
Elektronische ISSN: 1471-2350
DOI
https://doi.org/10.1186/s12881-019-0929-1

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