APA (7th ed.) Citation

Mercan, M., Seyhan, S., & Yayla, V. (2025). The phenotyping dilemma in VRK1-related motor neuron disease: A Turkish family with young-onset amyotrophic lateral sclerosis caused by a novel mutation. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 26(5/6), 573. https://doi.org/10.1080/21678421.2025.2477732

Chicago Style (17th ed.) Citation

Mercan, Metin, Serhat Seyhan, and Vildan Yayla. "The Phenotyping Dilemma in VRK1-related Motor Neuron Disease: A Turkish Family with Young-onset Amyotrophic Lateral Sclerosis Caused by a Novel Mutation." Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration 26, no. 5/6 (2025): 573. https://doi.org/10.1080/21678421.2025.2477732.

MLA (9th ed.) Citation

Mercan, Metin, et al. "The Phenotyping Dilemma in VRK1-related Motor Neuron Disease: A Turkish Family with Young-onset Amyotrophic Lateral Sclerosis Caused by a Novel Mutation." Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, vol. 26, no. 5/6, 2025, p. 573, https://doi.org/10.1080/21678421.2025.2477732.