WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype
Saved in:
Published in | Neurology. Genetics Vol. 4; no. 2; p. e227 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wolters Kluwer
01.04.2018
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 The Article Processing Charge was funded by Land Schleswig-Holstein within the funding programme Open Access Publikationsfonds. Funding information and disclosures are provided at the end of the article. Full disclosure form information provided by the authors is available with the full text of this article at Neurology.org/NG. |
---|---|
ISSN: | 2376-7839 2376-7839 |
DOI: | 10.1212/NXG.0000000000000227 |