Results

eNauka >  Results >  WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype
Title: WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype
Authors: Kulikovskaja, Leonora; Sarajlija, Adrijan  ; Savić Pavićević, Dušanka  ; Dobričić, Valerija ; Klein, Christine; Westenberger, Ana
Issue Date: 2018
Publication: Neurology. Genetics
ISSN: 2376-7839 Neurology-Genetics Search Idenfier
Publisher: [Hagerstown, MD] : Published for the American Academy of Neurology by Wolters Kluwer
Type: Article
Collation: vol. 4 br. 2 str. e227
DOI: 10.1212/nxg.0000000000000227
WoS-ID: 000430503200006
Scopus-ID: 2-s2.0-85048727177
PMID: 29600274
PMCID: PMC5873728
URI: https://enauka.gov.rs/handle/123456789/225027
URL: https://www.neurology.org/doi/10.1212/NXG.0000000000000227
Metadata source: Migrirano iz RIS podataka
M-category: 
Mp. category will be shown later

15
SCOPUSTM
8
PubMed CentralTM
10
OpenCitations
15
WEB OF SCIENCETM
Altmetric
Dimensions
Unpaywall

Items in eNauka are protected by copyright, with all rights reserved, unless otherwise indicated.