Work

The phenotyping dilemma in VRK1-related motor neuron disease: a Turkish family with young-onset amyotrophic lateral sclerosis caused by a novel mutation

Year: 2025

Type: article

Source: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

DOI: 10.1080/21678421.2025.2477732

Authors: Metin Mercan, Serhat Seyhan, Vildan Yayla

Institutions: Bakırköy Dr.Sadi Konuk Eğitim ve Araştırma Hastanesi, Memorial Sisli Hospital

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: W4408446479

FWCI: 0.712

Cites: 73

Cited by: 2

Related to: 10