Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Movement Disorders and SETX[original query] |
---|
Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes. Neurogenetics 2019 2 20 (1): 27-38. Elert-Dobkowska Ewelina, Stepniak Iwona, Krysa Wioletta, Ziora-Jakutowicz Karolina, Rakowicz Maria, Sobanska Anna, Pilch Jacek, Antczak-Marach Dorota, Zaremba Jacek, Sulek An |
Screening Gene Mutations in Chinese Patients With Benign Essential Blepharospasm. Frontiers in neurology 2020 2 10 1387. Dong Hongjuan, Luo Ying, Fan Shanghua, Yin Bo, Weng Chao, Peng B |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
- Content source: