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

Loading...
Thumbnail Image

relationships.isOrgUnitOf

Program

relationships.isAuthorOf

Author

Yücesan, Emrah

Yalnızoğlu, D

Oğuz, KK

Sağıroğlu, MŞ

Özbek, U

Serdaroğlu, E

Bilgiç, B

Erdem, S

İşeri, SAU

Advisor

Language

Publisher

Journal Title

Journal ISSN

Volume Title

Abstract

Description

Source

Keywords

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

Endorsement

Review

Supplemented By

Referenced By

5

Views

0

Downloads

View PlumX Details


Sustainable Development Goals