Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span.

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Yücel-Yılmaz D., Yücesan E., Yalnızoğlu D., Oğuz K., Sağıroğlu M., Özbek U., ...More

Brain & development, vol.40, pp.458-464, 2018 (SCI-Expanded)

• Publication Type: Article / Article
• Volume: 40
• Publication Date: 2018
• Doi Number: 10.1016/j.braindev.2018.02.013
• Journal Name: Brain & development
• Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
• Page Numbers: pp.458-464
• Bezmialem Vakıf University Affiliated: Yes