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Title:

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

Document type:
Correction
Author(s):
Blok, Lot Snijders; Rousseau, Justine; Twist, Joanna; Ehresmann, Sophie; Takaku, Motoki; Venselaar, Hanka; Rodan, Lance H.; Nowak, Catherine B.; Douglas, Jessica; Swoboda, Kathryn J.; Steeves, Marcie A.; Sahai, Inderneel; Stumpel, Connie T. R. M.; Stegmann, Alexander P. A.; Wheeler, Patricia; Willing, Marcia; Fiala, Elise; Kochhar, Aaina; Gibson, William T.; Cohen, Ana S. A.; Agbahovbe, Ruky; Innes, A. Micheil; Au, P. Y. Billie; Rankin, Julia; Anderson, Ilse J.; Skinner, Steven A.; Louie, Raymon...     »
Journal title abbreviation:
Nat Commun
Year:
2019
Journal volume:
10
Fulltext / DOI:
doi:10.1038/s41467-019-08800-2
Pubmed ID:
http://view.ncbi.nlm.nih.gov/pubmed/30770872
Print-ISSN:
2041-1723
TUM Institution:
Institut für Humangenetik
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