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

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

16

Citations

9

References

2018

Year

Didem Yücel‐Yılmaz, Emrah Yücesan, Dilek Yalnızoğlu, Kader Karlı Oğuz, Mahmut Şamil Sağıroğlu, Uğur Özbek, Esra Serdaroğlu, Sevim Erdem‐Özdamar, Haşmet Hanağası, Hakan Gürvıt,

Brain and Development

KinesiologyLife SpanGenetic DisorderKif1c Gene MutationsGeneticsMedicineClinical PhenotypeNeuropathologyNeuromuscular PathologyNeuromusculoskeletal Disorder

References

	Year	Citations

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