Results

eNauka >  Results >  Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene
Title: Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene
Authors: Kecmanović, Miljana  ; Jović, Nebojša ; Čukić, Mirjana; Keckarević Marković, Milica  ; Keckarević, Dušan  ; Stevanović, Galina; Romac, Stanka
Issue Date: 2013
Publication: Journal of the Neurological Sciences
ISSN: 0022-510X Journal of the Neurological Sciences Search Idenfier
Type: Article
Collation: vol. 325 br. 1-2 str. 170-173
DOI: 10.1016/j.jns.2012.12.006
WoS-ID: 000315323000033
Scopus-ID: 2-s2.0-84872896320
PMID: 23317923
URI: https://biore.bio.bg.ac.rs/handle/123456789/2573
https://enauka.gov.rs/handle/123456789/334689
Metadata source: Migracija
M-category: 
22M22

11
SCOPUSTM
6
PubMed CentralTM
11
OpenCitations
11
WEB OF SCIENCETM
Altmetric
Dimensions
Unpaywall

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