Work

Faculty Opinions recommendation of Exome sequencing reveals VCP mutations as a cause of familial ALS.

Year: 2011

Type: peer-review

Source: Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature

DOI: 10.3410/f.7862957.14078056

Author: Guy Rouleau

Institution: Montreal Neurological Institute and Hospital

Language: English

Topic: Amyotrophic Lateral Sclerosis Research

Subfield: Clinical Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W4235936829

Cites:

Cited by: 1

Related to: 10