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eNauka >  Results >  C9orf72 expansion as a possible genetic cause of Huntington disease phenocopy syndrome
Title: C9orf72 expansion as a possible genetic cause of Huntington disease phenocopy syndrome
Authors: Kostić, Vladimir ; Dobričić, Valerija; Stanković, Iva; Ralić, Vesna; Stefanova, Elka 
Issue Date: 2014
Publication: JOURNAL OF NEUROLOGY
ISSN: 0340-5354 Journal of Neurology Search Idenfier
Type: Article
Collation: vol. 261 br. 10 str. 1917-1921
DOI: 10.1007/s00415-014-7430-8
WoS-ID: 000343755300010
Scopus-ID: 2-s2.0-84914693305
URI: https://enauka.gov.rs/handle/123456789/414949
Project: Ministry of Education, Science, and Technological Development, Republic of Serbia [175090]
Metadata source: Migracija
M-category: 
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