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Estévez-Arias, B.* ; Matalonga, L.* ; Yubero, D.* ; Polavarapu, K.* ; Codina, A.E.* ; Ortez, C.* ; Carrera-García, L.* ; Expósito-Escudero, J.* ; Jou, C.* ; Meyer, S.* ; Kilicarslan, O.A.* ; Aleman, A.* ; Thompson, R.* ; Luknárová, R.* ; Esteve-Codina, A.* ; Gut, M.* ; Laurie, S.* ; Demidov, G.* ; Yépez, V.A.* ; Beltran, S.* ; Gagneur, J. ; Töpf, A.* ; Lochmüller, H.* ; Nascimento, A.* ; Hoenicka, J.* ; Palau, F.* ; Natera-de Benito, D.*

Correction: Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseases.

Eur. J. Hum. Genet., DOI: 10.1038/s41431-024-01756-y (2024)
Publ. Version/Full Text DOI PMC
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Open Access Green as soon as Postprint is submitted to ZB.
Correction to: European Journal of Human Geneticshttps://doi.org/10.1038/s41431-024-01699-4, published online 27 September 2024 In the original article was a typo in Table 1 for patient 17. The correct variant is “c.33055del (p.Glu11019Serfs*21)” instead of “c.32104del (p.Ser10702LeufsTer6)” The original article has been corrected.
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Publication type Other: Correction, Addition
Language english
Publication Year 2024
HGF-reported in Year 2024
ISSN (print) / ISBN 1018-4813
e-ISSN 1476-5438
Journal European Journal of Human Genetics
Publisher Nature Publishing Group
Reviewing status Peer reviewed
Institute(s) Institute of Computational Biology (ICB)
POF-Topic(s) 30205 - Bioengineering and Digital Health
Research field(s) Enabling and Novel Technologies
PSP Element(s) G-503800-001
DOI 10.1038/s41431-024-01756-y
Scopus ID 85212185284
PubMed ID 39658675
Erfassungsdatum 2024-12-12
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