Correction: Homozygosity mapping provides supporting evidence of pathogenicity in recessive Mendelian disease.


Journal

Genetics in medicine : official journal of the American College of Medical Genetics
ISSN: 1530-0366
Titre abrégé: Genet Med
Pays: United States
ID NLM: 9815831

Informations de publication

Date de publication:
03 2019
Historique:
pubmed: 18 11 2018
medline: 18 11 2018
entrez: 18 11 2018
Statut: ppublish

Résumé

The original version of this Article contained an error in the top left of Figure 2: the number 1 on the y-axis had been changed to 0 during the typesetting process. This has now been corrected in both the PDF and HTML versions of the Article.

Identifiants

pubmed: 30446706
doi: 10.1038/s41436-018-0357-1
pii: S1098-3600(21)01045-5
pmc: PMC6752275
doi:

Types de publication

Journal Article Published Erratum

Langues

eng

Pagination

766

Commentaires et corrections

Type : ErratumFor

Auteurs

Matthew Neil Wakeling (MN)

Institute of Biomedical & Clinical Science, University of Exeter, Exeter, UK. m.wakeling@exeter.ac.uk.

Thomas William Laver (TW)

Institute of Biomedical & Clinical Science, University of Exeter, Exeter, UK.

Caroline Fiona Wright (CF)

Institute of Biomedical & Clinical Science, University of Exeter, Exeter, UK.

Elisa De Franco (E)

Institute of Biomedical & Clinical Science, University of Exeter, Exeter, UK.

Karen Lucy Stals (KL)

Department of Molecular Genetics, Royal Devon & Exeter NHS Foundation Trust, Exeter, UK.

Ann-Marie Patch (AM)

QIMR Berghofer, Herston, Queensland, Australia.

Andrew Tym Hattersley (AT)

Institute of Biomedical & Clinical Science, University of Exeter, Exeter, UK.

Sarah Elizabeth Flanagan (SE)

Institute of Biomedical & Clinical Science, University of Exeter, Exeter, UK.

Sian Ellard (S)

Institute of Biomedical & Clinical Science, University of Exeter, Exeter, UK.
Department of Molecular Genetics, Royal Devon & Exeter NHS Foundation Trust, Exeter, UK.

Classifications MeSH