Erratum: Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001))

Brooke Sadler, Jackson Wilborn, Lilian Antunes, Timothy Kuensting, Andrew T. Hale, Stephen R. Gannon, Kevin McCall, Carlos Cruchaga, Matthew Harms, Norine Voisin, Alexandre Reymond, Gerarda Cappuccio, Nicola Brunetti-Pierri, Marco Tartaglia, Marcello Niceta, Chiara Leoni, Giuseppe Zampino, Allison Ashley-Koch, Aintzane Urbizu, Melanie E. GarrettKaren Soldano, Alfons Macaya, Donald Conrad, Jennifer Strahle, Matthew B. Dobbs, Tychele N. Turner, Chevis N. Shannon, Douglas Brockmeyer, David D. Limbrick, Christina A. Gurnett, Gabe Haller

Research output: Contribution to journalComment/debatepeer-review

Abstract

(The American Journal of Human Genetics 108, 100–114; January 7, 2021) In the originally published version of this article, the name of author Nicola Brunetti-Pierri was misspelled. This has been corrected online. The authors regret this error.

Original languageEnglish (US)
Pages (from-to)368
Number of pages1
JournalAmerican Journal of Human Genetics
Volume108
Issue number2
DOIs
StatePublished - Feb 4 2021

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Fingerprint

Dive into the research topics of 'Erratum: Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001))'. Together they form a unique fingerprint.

Cite this