Work

C9orf72 expansion as a possible genetic cause of Huntington disease phenocopy syndrome

Year: 2014

Type: article

Study design: Observational Study

Source: Journal of Neurology

DOI: 10.1007/s00415-014-7430-8

Authors: Vladimir S. Kostić, Valerija Dobričić, Iva Stanković, Vesna Ralić, Elka Stefanova

Institution: University of Belgrade

Language: English

Topic: Genetic Neurodegenerative Diseases

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Science and Engineering Research Board

OpenAlex ID: W2130529099

FWCI: 1.958

Cites: 13

Cited by: 37

Related to: 10