İNCECİK, F. And HERGÜNER, M. Ö. 2022. Hereditary spastic paraplegia type 26 with a novel mutation in B4GALNT1 gene and literature review of the clinical features. 17. International Child Neurology Congress , (Antalya, Turkey).

İNCECİK, F., & HERGÜNER, M. Ö., (2022). Hereditary spastic paraplegia type 26 with a novel mutation in B4GALNT1 gene and literature review of the clinical features . 17. International Child Neurology Congress, Antalya, Turkey

İNCECİK, FARUK, And M.ÖZLEM HERGÜNER. "Hereditary spastic paraplegia type 26 with a novel mutation in B4GALNT1 gene and literature review of the clinical features," 17. International Child Neurology Congress, Antalya, Turkey, 2022

İNCECİK, FARUK And HERGÜNER, M.ÖZLEM. "Hereditary spastic paraplegia type 26 with a novel mutation in B4GALNT1 gene and literature review of the clinical features." 17. International Child Neurology Congress , Antalya, Turkey, 2022

İNCECİK, F. And HERGÜNER, M. Ö. (2022) . "Hereditary spastic paraplegia type 26 with a novel mutation in B4GALNT1 gene and literature review of the clinical features." 17. International Child Neurology Congress , Antalya, Turkey.

@conferencepaper{conferencepaper, author={FARUK İNCECİK And author={M.ÖZLEM HERGÜNER}, title={Hereditary spastic paraplegia type 26 with a novel mutation in B4GALNT1 gene and literature review of the clinical features}, congress name={17. International Child Neurology Congress}, city={Antalya}, country={Turkey}, year={2022}}