Corrigendum to “Restless legs syndrome in NKX2-1-related chorea: An expansion of the disease spectrum” (Brain and Development (2019) 41(3) (250–256), (S0387760418304959), (10.1016/j.braindev.2018.10.001))

A. Iodice*, M. Carecchio, G. Zorzi, B. Garavaglia, C. Spagnoli, G. G. Salerno, D. Frattini, N. E. Mencacci, F. Invernizzi, L. Veneziano, E. Mantuano, M. Angriman, C. Fusco

*Corresponding author for this work

Research output: Contribution to journalComment/debate

Abstract

The authors would like to revise the printed version of the above article, because it contained an error regarding gene nomenclature in one mutation reported. In the section “Results” and in Table 2, we described a mutation in NKX2-1 (NM_001079668.2) c.300C>G p.Tyr100*, although c.300 is a G not a C and codon 100 is ATG coding for Met not Tyr. For that reason we would like to specify that the reported mutation was referred to the “short” form of the protein (NM_003317) while the correct numbering referred to the “long” form (NM_001079668.2) is p.Tyr130* c.390C>G. The authors would like to apologise for any inconvenience caused.

Original languageEnglish (US)
Pages (from-to)643
Number of pages1
JournalBrain and Development
Volume41
Issue number7
DOIs
StatePublished - Aug 2019

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Developmental Neuroscience
  • Clinical Neurology

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