Work

Novel mitofusin 2 splice-site mutation causes Charcot–Marie–Tooth disease type 2 with prominent sensory dysfunction

Year: 2014

Type: article

Study design: Case Report

Source: Neuromuscular Disorders

DOI: 10.1016/j.nmd.2014.01.007

Authors: Mika H. Martikainen, Laura Kytövuori, Kari Majamaa

Institutions: University of Turku, Turku University Hospital, Oulu University Hospital, University of Oulu

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

OpenAlex ID: W2020657653

FWCI: 0.245

Cites: 27

Cited by: 6

Related to: 10