Correction: GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder (Genetics in Medicine, (2020), 10.1038/s41436-019-0747-z)

The Undiagnosed Diseases Network

doi:10.1038/s41436-020-0760-2

Correction: GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder (Genetics in Medicine, (2020), 10.1038/s41436-019-0747-z)

The Undiagnosed Diseases Network

University of California at Los Angeles
University of Sydney
Cedars-Sinai Medical Center
Medical College of Wisconsin
Hofstra North Shore-LIJ School of Medicine
University of Texas Southwestern Medical Center
East Tennessee State University
Geisinger Medical Center
Brooke Army Medical Center
University of Texas Health Science Center
Johns Hopkins University
Hospital of the King's Daughters
Kennedy Krieger Institute
University of Lisbon
Geisinger Autism & Developmental Medicine Institute
Children's Minnesota
Children's Hospital of Wisconsin Wauwatosa
University of South Florida
Maine Medical Center
Joe DiMaggio Childrens Hospital
Royal North Shore Hospital
Sanford Children’s Specialty Clinic
University of South Dakota
University of Toronto
Nemours Children's Health System
Children's National Medical Center
Duke University
Cincinnati Children's Hospital Medical Center
University of Cincinnati
Manchester University NHS Foundation Trust
Newcastle upon Tyne Hospitals NHS Foundation Trust
University of Southampton
University Hospital Southampton NHS Foundation Trust
Belfast Health and Social Care Trust
Great Ormond Street Hospital for Children NHS Foundation Trust
University of Edinburgh
West Midlands Regional Clinical Genetics Service and Birmingham Health Partners
Birmingham Women's and Children's NHS Foundation Trust
University of Ottawa
University of Miami
University of Pennsylvania

Producción científica

2 Citas (Scopus)

Resumen

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Idioma original	English
Páginas (desde-hasta)	822
Número de páginas	1
Publicación	Genetics in Medicine
Volumen	22
N.º	4
DOI	https://doi.org/10.1038/s41436-020-0760-2
Estado	Published - 1 abr 2020

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10.1038/s41436-020-0760-2

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https://www.scopus.com/pages/publications/85079441963

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@article{24f456a74a514a9d9f1ca43fe94bf979,

title = "Correction: GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder (Genetics in Medicine, (2020), 10.1038/s41436-019-0747-z)",

abstract = "An amendment to this paper has been published and can be accessed via a link at the top of the paper.",

author = "\{The Undiagnosed Diseases Network\} and Christine Shieh and Natasha Jones and Brigitte Vanle and Margaret Au and Huang, \{Alden Y.\} and Silva, \{Ana P.G.\} and Hane Lee and Douine, \{Emilie D.\} and Otero, \{Maria G.\} and Andrew Choi and Katheryn Grand and Taff, \{Ingrid P.\} and Delgado, \{Mauricio R.\} and Hajianpour, \{M. J.\} and Andrea Seeley and Luis Rohena and Hilary Vernon and Gripp, \{Karen W.\} and Vergano, \{Samantha A.\} and Sonal Mahida and Sakkubai Naidu and Sousa, \{Ana Berta\} and Wain, \{Karen E.\} and Challman, \{Thomas D.\} and Geoffrey Beek and Donald Basel and Judith Ranells and Rosemarie Smith and Roman Yusupov and Freckmann, \{Mary Louise\} and Lisa Ohden and Laura Davis-Keppen and David Chitayat and Dowling, \{James J.\} and Richard Finkel and Andrew Dauber and Rebecca Spillmann and Pena, \{Loren D.M.\} and Kay Metcalfe and Miranda Splitt and Katherine Lachlan and McKee, \{Shane A.\} and Jane Hurst and Fitzpatrick, \{David R.\} and Morton, \{Jenny E.V.\} and Helen Cox and Sunita Venkateswaran and Young, \{Juan I.\} and Marsh, \{Eric D.\} and Nelson, \{Stanley F.\}",

note = "Publisher Copyright: {\textcopyright} 2020, American College of Medical Genetics and Genomics.",

year = "2020",

month = apr,

day = "1",

doi = "10.1038/s41436-020-0760-2",

language = "English",

volume = "22",

pages = "822",

journal = "Genetics in Medicine",

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TY - JOUR

T1 - Correction

T2 - GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder (Genetics in Medicine, (2020), 10.1038/s41436-019-0747-z)

AU - The Undiagnosed Diseases Network

AU - Shieh, Christine

AU - Jones, Natasha

AU - Vanle, Brigitte

AU - Au, Margaret

AU - Huang, Alden Y.

AU - Silva, Ana P.G.

AU - Lee, Hane

AU - Douine, Emilie D.

AU - Otero, Maria G.

AU - Choi, Andrew

AU - Grand, Katheryn

AU - Taff, Ingrid P.

AU - Delgado, Mauricio R.

AU - Hajianpour, M. J.

AU - Seeley, Andrea

AU - Rohena, Luis

AU - Vernon, Hilary

AU - Gripp, Karen W.

AU - Vergano, Samantha A.

AU - Mahida, Sonal

AU - Naidu, Sakkubai

AU - Sousa, Ana Berta

AU - Wain, Karen E.

AU - Challman, Thomas D.

AU - Beek, Geoffrey

AU - Basel, Donald

AU - Ranells, Judith

AU - Smith, Rosemarie

AU - Yusupov, Roman

AU - Freckmann, Mary Louise

AU - Ohden, Lisa

AU - Davis-Keppen, Laura

AU - Chitayat, David

AU - Dowling, James J.

AU - Finkel, Richard

AU - Dauber, Andrew

AU - Spillmann, Rebecca

AU - Pena, Loren D.M.

AU - Metcalfe, Kay

AU - Splitt, Miranda

AU - Lachlan, Katherine

AU - McKee, Shane A.

AU - Hurst, Jane

AU - Fitzpatrick, David R.

AU - Morton, Jenny E.V.

AU - Cox, Helen

AU - Venkateswaran, Sunita

AU - Young, Juan I.

AU - Marsh, Eric D.

AU - Nelson, Stanley F.

PY - 2020/4/1

Y1 - 2020/4/1

N2 - An amendment to this paper has been published and can be accessed via a link at the top of the paper.

AB - An amendment to this paper has been published and can be accessed via a link at the top of the paper.

UR - https://www.scopus.com/pages/publications/85079441963

U2 - 10.1038/s41436-020-0760-2

DO - 10.1038/s41436-020-0760-2

M3 - Comment/debate

C2 - 32047287

AN - SCOPUS:85079441963

SN - 1098-3600

VL - 22

SP - 822

JO - Genetics in Medicine

JF - Genetics in Medicine

IS - 4

ER -

Correction: GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder (Genetics in Medicine, (2020), 10.1038/s41436-019-0747-z)

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