WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype

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Published inNeurology. Genetics Vol. 4; no. 2; p. e227
Main Authors Kulikovskaja, Leonora, Sarajlija, Adrijan, Savic-Pavicevic, Dusanka, Dobricic, Valerija, Klein, Christine, Westenberger, Ana
Format Journal Article
LanguageEnglish
Published United States Wolters Kluwer 01.04.2018
Subjects
Clinical/Scientific Notes
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Author Klein, Christine
Savic-Pavicevic, Dusanka
Sarajlija, Adrijan
Kulikovskaja, Leonora
Westenberger, Ana
Dobricic, Valerija
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Cites_doi 10.1038/ejhg.2015.274
10.1038/nature19057
10.1016/j.ajhg.2012.10.019
10.1038/ng.2562
10.1016/j.mcp.2016.01.003
10.1177/0883073807309786
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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.
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Zarate YA (e_1_3_4_8_2) 2016; 24
e_1_3_4_7_2
e_1_3_4_6_2
Allen RC (e_1_3_4_5_2) 1992; 51
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References_xml – volume: 24
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  publication-title: Eur J Hum Genet
  doi: 10.1038/ejhg.2015.274
  contributor:
    fullname: Zarate YA
– ident: e_1_3_4_6_2
  doi: 10.1038/nature19057
– ident: e_1_3_4_2_2
  doi: 10.1016/j.ajhg.2012.10.019
– ident: e_1_3_4_3_2
  doi: 10.1038/ng.2562
– ident: e_1_3_4_4_2
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  article-title: Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation
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  doi: 10.1177/0883073807309786
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Title WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype
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