Work

Neuronal loss in Pelizaeus–Merzbacher disease differs in various mutations of the proteolipid protein 1

Year: 2009

Type: article

Study design: Case Report

Source: Acta Neuropathologica

DOI: 10.1007/s00401-009-0562-8

Authors: Anders A. F. Sima, Christopher R. Pierson, Randall L. Woltjer, Grace M. Hobson, Jeffrey A. Golden, William J. Kupsky, Galen M. Schauer, Thomas D. Bird, Robert P. Skoff, James Y. Garbern

Institutions: Wayne State University, Oregon Health & Science University, Alfred I. duPont Hospital for Children, Children's Hospital of Philadelphia, University of Pennsylvania, Kaiser Permanente, Kaiser Permanente Oakland Medical Center, University of Washington

Language: English

Topic: Hereditary Neurological Disorders

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: National Institute of Neurological Disorders and Stroke, National Center for Research Resources

Awards: G1598762266, Center for Pediatric Research, Molecular genetics of Pelizaeus-Merzbacher disease, Molecular Mechanisms of Neurodegeneration

OpenAlex ID: W2159737799

FWCI: 1.244

Cites: 46

Cited by: 50

Related to: 10