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Erschienen in: Orphanet Journal of Rare Diseases 1/2019

Open Access 01.12.2019 | Correction

Correction to: Bisphosphonate therapy for spinal osteoporosis in Hajdu-Cheney syndrome – new data and literature review

verfasst von: James F. H. Pittaway, Christopher Harrison, Yumie Rhee, Muriel Holder-Espinasse, Alan E. Fryer, Tim Cundy, William M. Drake, Melita D. Irving

Erschienen in: Orphanet Journal of Rare Diseases | Ausgabe 1/2019

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The original article can be found online at https://​doi.​org/​10.​1186/​s13023-018-0795-5
Correction to: Orphanet J Rare Dis
https://doi.org/10.1186/s13023-018-0795-5
After publication of this article [1], it is noticed reference no. 17 was incorrectly provided, details are shown below:
Original reference no. 17:
Canalis E, Schilling L, Yee SP, Lee SK, Zanotti S. Hajdu Cheney mouse mutants exhibit osteopenia, increased Osteoclastogenesis, and bone resorption. J Biol Chem. 2016;291(4):1538–51. https://​doi.​org/​10.​1074/​jbc. M115.685453.
Correct reference no. 17:
G. Adami, M. Rossini, D. Gatti, G. Orsolini, L. Idolazzi, O. Viapiana, A. Scarpa, E. Canalis Hajdu Cheney Syndrome; report of a novel NOTCH2 mutation and treatment with denosumab Bone, 92 (2016), pp. 150–156.
The author apologizes for the inconvenience caused.
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: Bisphosphonate therapy for spinal osteoporosis in Hajdu-Cheney syndrome – new data and literature review
verfasst von
James F. H. Pittaway
Christopher Harrison
Yumie Rhee
Muriel Holder-Espinasse
Alan E. Fryer
Tim Cundy
William M. Drake
Melita D. Irving
Publikationsdatum
01.12.2019
Verlag
BioMed Central
Erschienen in
Orphanet Journal of Rare Diseases / Ausgabe 1/2019
Elektronische ISSN: 1750-1172
DOI
https://doi.org/10.1186/s13023-019-1084-7

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