Open Access 01.12.2019 | Correction
Correction to: Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10
Erschienen in: BMC Medical Genetics | Ausgabe 1/2019
Correction to: BMC Med Genet (2019) 20:166
https://doi.org/10.1186/s12881-019-0895-7
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Please be advised that following publication of the original article [1], the authors have identified the following errors with the scientific content:
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
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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.
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