Open Access

Erratum to: Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family

  • Vito Guarnieri1Email author,
  • Raewyn M. Seaberg2,
  • Catherine Kelly3, 4,
  • M. Jean Davidson5,
  • Simon Raphael6,
  • Andrew Y. Shuen7,
  • Filomena Baorda1,
  • Orazio Palumbo1,
  • Alfredo Scillitani8,
  • Geoffrey N. Hendy9, 10 and
  • David E.C. Cole7
BMC Medical GeneticsBMC series – open, inclusive and trusted201718:99

Received: 7 September 2017

Accepted: 7 September 2017

Published: 13 September 2017

The original article was published in BMC Medical Genetics 2017 18:83


Following publication of the original article [1], the authors identified the following errors in the scientific content:

p.4, para. 3: “(1 tablet/10 mL RIPA)” should read “(1 tablet/10 mL RIPA buffer)”.

p.4, para. 4: “II-1” should read “II-2”.

Minor mistakes were also identified in the table on page 6, and in the Abbreviations section on page 7.

The original article has been corrected.



Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, 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 ( applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

Medical Genetics, IRCCS Casa Sollievo della Sofferenza Hospital
Department of Otolaryngology - Head and Neck Surgery, University of Toronto
Department of Medicine, University of Toronto
Division of Endocrinology, Women’s College Hospital
Department of Otolaryngology, Head & Neck Surgery, Sunnybrook Health Sciences Centre
Department of Anatomic Pathology, Sunnybrook Health Sciences Centre
Departments of Laboratory Medicine and Pathobiology, Medicine and Genetics, University of Toronto
Endocrinology, IRCCS Casa Sollievo della Sofferenza Hospital
Metabolic Disorders and Complications, McGill University Health Centre-Research Institute
Departments of Medicine, Physiology and Human Genetics, McGill University


  1. Guarnieri V, Seaberg RM, Kelly C, Jean Davidson M, Raphael S, Shuen AY, Baorda F, Palumbo O, Scillitani A, Hendy GN, Cole DEC. Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family. BMC Med Genet. 2017;18:83. doi:10.1186/s12881-017-0445-0.View ArticlePubMedPubMed CentralGoogle Scholar


© The Author(s). 2017