Work

Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene

Year: 2000

Type: article

Study design: Observational Study

Source: Neurology

DOI: 10.1212/wnl.55.9.1267

Authors: S.C. Blumen, A.D. Korczyn, H. Lavoie, S. Medynski, J. Chapman, A. Asherov, P. Nisipeanu, R. Inzelberg, R.L. Carasso, J.-P. Bouchard, F.M. S. Tomé, G.A. Rouleau, B. Brais

Institutions: Tel Aviv University, Technion – Israel Institute of Technology, Hillel Yaffe Medical Center, Université de Montréal

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: Hebrew University of Jerusalem

OpenAlex ID: W2145961280

FWCI: 0.931

Cites: 21

Cited by: 54

Related to: 10