Work

Association of UBQLN1 mutation with Brown–Vialetto–Van Laere syndrome but not typical ALS

Year: 2012

Type: article

Study design: Observational Study

Source: Neurobiology of Disease

DOI: 10.1016/j.nbd.2012.06.018

Authors: Paloma González-Pérez, Yubing Lu, Ru-Ju Chian, Peter C. Sapp, Rudolph E. Tanzi, Lars Bertram, Diane McKenna-Yasek, Fen-Biao Gao, Robert H. Brown

Institutions: University of Massachusetts Chan Medical School, Massachusetts General Hospital, Max Planck Society, Max Planck Institute for Molecular Genetics

Language: German

Topic: Amyotrophic Lateral Sclerosis Research

Subfield: Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: National Institutes of Health, National Institute of Neurological Disorders and Stroke

Awards: G1050801880, Animal Models for Studying Human Frontotemporal Dementia, High-Throughput Genomic Approaches to Identify ALS Genes, Full Human Genome Sequencing in ALS

OpenAlex ID: W2130110370

FWCI: 1.669

Cites: 42

Cited by: 27

Related to: 10