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

Wakeling, Matthew Neil; Laver, Thomas William; Wright, Caroline Fiona; De Franco, Elisa; Stals, Karen Lucy; Patch, Ann-Marie; Hattersley, Andrew Tym; Flanagan, Sarah Elizabeth; Ellard, Sian

Wakeling, Matthew Neil; Laver, Thomas William; Wright, Caroline Fiona; De Franco, Elisa; Stals, Karen Lucy; Patch, Ann-Marie; Hattersley, Andrew Tym; Flanagan, Sarah Elizabeth; Ellard, Sian.

Afiliación

Wakeling MN; Institute of Biomedical & Clinical Science, University of Exeter, Exeter, UK. m.wakeling@exeter.ac.uk.
Laver TW; Institute of Biomedical & Clinical Science, University of Exeter, Exeter, UK.
Wright CF; Institute of Biomedical & Clinical Science, University of Exeter, Exeter, UK.
De Franco E; Institute of Biomedical & Clinical Science, University of Exeter, Exeter, UK.
Stals KL; Department of Molecular Genetics, Royal Devon & Exeter NHS Foundation Trust, Exeter, UK.
Patch AM; QIMR Berghofer, Herston, Queensland, Australia.
Hattersley AT; Institute of Biomedical & Clinical Science, University of Exeter, Exeter, UK.
Flanagan SE; Institute of Biomedical & Clinical Science, University of Exeter, Exeter, UK.
Ellard S; Institute of Biomedical & Clinical Science, University of Exeter, Exeter, UK.

Genet Med ; 21(3): 766, 2019 03.

Article en En | MEDLINE | ID: mdl-30446706

RESUMEN

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.

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos

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