Work

A variant of Nesprin1 giant devoid of KASH domain underlies the molecular etiology of autosomal recessive cerebellar ataxia type I

Year: 2015

Type: article

Source: Neurobiology of Disease

DOI: 10.1016/j.nbd.2015.03.027

Authors: David Razafsky, Didier Hodzic

Institution: Washington University in St. Louis

Language: English

Topic: Nuclear Structure and Function

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: Research to Prevent Blindness, Hope Center for Neurological Disorders, National Institutes of Health, McDonnell Center for Cellular and Molecular Neurobiology, Washington University in St. Louis, National Eye Institute, National Center for Research Resources

Awards: G1882013177, Core Grant for Vision Research, NUCLEAR DYNAMICS IN RETINAL DEVELOPMENT AND HOMEOSTASIS

OpenAlex ID: W2053366875

FWCI: 2.892

Cites: 43

Cited by: 42

Related to: 10