Work

SET binding factor 2 (SBF2) mutation causes CMT4B with juvenile onset glaucoma

Year: 2004

Type: article

Source: Neurology

DOI: 10.1212/01.wnl.0000133211.40288.9a

Authors: R. Hirano, H. Takashima, F. Umehara, H. Arimura, K. Michizono, Y. Okamoto, M. Nakagawa, C. F. Boerkoel, J. R. Lupski, M. Osame, K. Arimura

Institutions: Kagoshima University, Baylor College of Medicine, Kyoto Prefectural University of Medicine

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: closed

Funders: Kagoshima University, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Neurological Disorders and Stroke

Awards: G2875609050, G541618229, A MURINE MODEL OF SMITH-MAGENIS SYNDROME, CMT Peripheral Neuropathy: IV. Genes and Pathogenesis

OpenAlex ID: W2130660232

FWCI: 1.055

Cites: 11

Cited by: 43

Related to: 10