CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018)

DDD Study

doi:10.1038/s41467-019-08800-2

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018)

DDD Study

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Original language	English
Article number	2079
Number of pages	4
Journal	Nature Communications
Volume	10
DOIs	https://doi.org/10.1038/s41467-019-08800-2
Publication status	Published - 2-May-2019

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and languageFinal publisher's version, 492 KBLicence: CC BY

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@article{2cb74c3477d440ac8c0e5f692009d7eb,

title = "CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018)",

author = "\{DDD Study\} and Blok, \{Lot Snijders\} and Justine Rousseau and Joanna Twist and Sophie Ehresmann and Motoki Takaku and Hanka Venselaar and Rodan, \{Lance H.\} and Nowak, \{Catherine B.\} and Jessica Douglas and Swoboda, \{Kathryn J.\} and Steeves, \{Marcie A.\} and Inderneel Sahai and Stumpel, \{Connie T. R. M.\} and Stegmann, \{Alexander P. A.\} and Patricia Wheeler and Marcia Willing and Elise Fiala and Aaina Kochhar and Gibson, \{William T.\} and Cohen, \{Ana S. A.\} and Ruky Agbahovbe and Innes, \{A. Micheil\} and Au, \{P. Y. Billie\} and Julia Rankin and Anderson, \{Ilse J.\} and Skinner, \{Steven A.\} and Louie, \{Raymond J.\} and Warren, \{Hannah E.\} and Alexandra Afenjar and Boris Keren and Caroline Nava and Julien Buratti and Arnaud Isapof and Diana Rodriguez and Raymond Lewandowski and Jennifer Propst and \{van Essen\}, Ton and Murim Choi and Sangmoon Lee and Chae, \{Jong H.\} and Susan Price and Schnur, \{Rhonda E.\} and Ganka Douglas and Wentzensen, \{Ingrid M.\} and Christiane Zweier and Andre Reis and Bialer, \{Martin G.\} and Christine Moore and Sandra Jansen and \{de Vries\}, Dylan",

year = "2019",

month = may,

day = "2",

doi = "10.1038/s41467-019-08800-2",

language = "English",

volume = "10",

journal = "Nature Communications",

issn = "2041-1723",

publisher = "Nature Publishing Group",

}

TY - JOUR

T1 - CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018)

AU - DDD Study

AU - Blok, Lot Snijders

AU - Rousseau, Justine

AU - Twist, Joanna

AU - Ehresmann, Sophie

AU - Takaku, Motoki

AU - Venselaar, Hanka

AU - Rodan, Lance H.

AU - Nowak, Catherine B.

AU - Douglas, Jessica

AU - Swoboda, Kathryn J.

AU - Steeves, Marcie A.

AU - Sahai, Inderneel

AU - Stumpel, Connie T. R. M.

AU - Stegmann, Alexander P. A.

AU - Wheeler, Patricia

AU - Willing, Marcia

AU - Fiala, Elise

AU - Kochhar, Aaina

AU - Gibson, William T.

AU - Cohen, Ana S. A.

AU - Agbahovbe, Ruky

AU - Innes, A. Micheil

AU - Au, P. Y. Billie

AU - Rankin, Julia

AU - Anderson, Ilse J.

AU - Skinner, Steven A.

AU - Louie, Raymond J.

AU - Warren, Hannah E.

AU - Afenjar, Alexandra

AU - Keren, Boris

AU - Nava, Caroline

AU - Buratti, Julien

AU - Isapof, Arnaud

AU - Rodriguez, Diana

AU - Lewandowski, Raymond

AU - Propst, Jennifer

AU - van Essen, Ton

AU - Choi, Murim

AU - Lee, Sangmoon

AU - Chae, Jong H.

AU - Price, Susan

AU - Schnur, Rhonda E.

AU - Douglas, Ganka

AU - Wentzensen, Ingrid M.

AU - Zweier, Christiane

AU - Reis, Andre

AU - Bialer, Martin G.

AU - Moore, Christine

AU - Jansen, Sandra

AU - de Vries, Dylan

PY - 2019/5/2

Y1 - 2019/5/2

U2 - 10.1038/s41467-019-08800-2

DO - 10.1038/s41467-019-08800-2

M3 - Article

SN - 2041-1723

VL - 10

JO - Nature Communications

JF - Nature Communications

M1 - 2079

ER -