The phenotyping dilemma in VRK1-related motor neuron disease: a Turkish family with young-onset amyotrophic lateral sclerosis caused by a novel mutation.
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| Title: | The phenotyping dilemma in VRK1-related motor neuron disease: a Turkish family with young-onset amyotrophic lateral sclerosis caused by a novel mutation. |
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| Authors: | Mercan, Metin1 (AUTHOR) dr_metin_mercan@hotmail.com, Seyhan, Serhat2 (AUTHOR), Yayla, Vildan1 (AUTHOR) |
| Source: | Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. Aug2025, Vol. 26 Issue 5/6, p573-590. 18p. |
| Database: | Academic Search Ultimate |
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| ISSN: | 21678421 |
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| DOI: | 10.1080/21678421.2025.2477732 |
