Erratum: 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

Vito Guarnieri, Raewyn M. Seaberg, Catherine Kelly, M. Jean Davidson, Simon Raphael, Andrew Y. Shuen, Filomena Baorda, Orazio Palumbo, Alfredo Scillitani, Geoffrey N. Hendy, David E.C. Cole

Research output: Contribution to journalComment/debate

1 Citation (Scopus)

Abstract

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.

Original languageEnglish
Article number99
JournalBMC Medical Genetics
Volume18
Issue number1
DOIs
Publication statusPublished - Sep 13 2017

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Viverridae
Tablets
Exons
Publications
Buffers
Hyperparathyroidism 2

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Erratum : 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. / Guarnieri, Vito; Seaberg, Raewyn M.; Kelly, Catherine; Jean Davidson, M.; Raphael, Simon; Shuen, Andrew Y.; Baorda, Filomena; Palumbo, Orazio; Scillitani, Alfredo; Hendy, Geoffrey N.; Cole, David E.C.

In: BMC Medical Genetics, Vol. 18, No. 1, 99, 13.09.2017.

Research output: Contribution to journalComment/debate

Guarnieri, Vito ; Seaberg, Raewyn M. ; Kelly, Catherine ; Jean Davidson, M. ; Raphael, Simon ; Shuen, Andrew Y. ; Baorda, Filomena ; Palumbo, Orazio ; Scillitani, Alfredo ; Hendy, Geoffrey N. ; Cole, David E.C. / Erratum : 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. In: BMC Medical Genetics. 2017 ; Vol. 18, No. 1.
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