Work

GJC2 promoter mutations causing Pelizaeus–Merzbacher-like disease

Year: 2013

Type: article

Source: Molecular Genetics and Metabolism

DOI: 10.1016/j.ymgme.2013.12.001

Authors: Leo Gotoh, Ken Inoue, Guy Helman, Sara Mora, Kiran Maski, Janet S. Soul, Miriam Bloom, Sarah H. Evans, Yu-ichi Goto, Ljubica Caldovic, Grace M. Hobson, Adeline Vanderver

Institutions: National Center of Neurology and Psychiatry, National Institute of Neuroscience, Children's National, Alfred I. duPont Hospital for Children, Boston Children's Hospital, Harvard University, University of Delaware, Thomas Jefferson University

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 Institutes of Health, Japan Society for the Promotion of Science, National Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: Treatment of congenital hypomyelinating leukodystrophy using the gene suppression effect of morpholino, Molecular genetics of Pelizaeus-Merzbacher disease, G5953875955, Intellectual and Developmental Disablities Research Center

OpenAlex ID: W2018042406

FWCI: 0.817

Cites: 21

Cited by: 21

Related to: 10