Work

X-linked spinocerebellar ataxia (SCA) type 1A: a novel late onset phenotype of the ATP2B3 mutation (P5.392)

Year: 2016

Type: article

Study design: Case Report

Source: Neurology

DOI: 10.1212/wnl.86.16_supplement.p5.392

Authors: Christopher Stephen, Kathleen Sweadner, John Penniston, Jeremy Schmahmann

Institutions: Harvard University, Massachusetts General Hospital

Language: English

Topic: Genetic Neurodegenerative Diseases

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2483991418

FWCI:

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Related to: 10