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

No Thumbnail Available
Date
2018-06-01T00:00:00Z
Authors
Yücel-Yılmaz, D
Yücesan, Emrah
Yalnızoğlu, D
Oğuz, KK
Sağıroğlu, MŞ
Özbek, U
Serdaroğlu, E
Bilgiç, B
Erdem, S
İşeri, SAU
Journal Title
Journal ISSN
Volume Title
Publisher
Research Projects
Organizational Units
Journal Issue

Metrics

Search on Google Scholar

Abstract
Description
Keywords
Citation
Yücel-Yılmaz D., Yücesan E., Yalnızoğlu D., Oğuz K., Sağıroğlu M., Özbek U., Serdaroğlu E., Bilgiç B., Erdem S., İşeri S., et al., -Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span.-, Brain & development, cilt.40, ss.458-464, 2018
Page Views

0

File Downloads

0

Sustainable Development Goals