İNCECİK, F. Et Al. 2022. Homozygous mutation in CWF19L1 with recessive ataxia syndrome in a Turkish child. 17. International Child Neurology Congress , (Antalya, Turkey).

İNCECİK, F., HERGÜNER, M. Ö., & TUĞ BOZDOĞAN, S., (2022). Homozygous mutation in CWF19L1 with recessive ataxia syndrome in a Turkish child . 17. International Child Neurology Congress, Antalya, Turkey

İNCECİK, FARUK, M.ÖZLEM HERGÜNER, And SEVCAN TUĞ BOZDOĞAN. "Homozygous mutation in CWF19L1 with recessive ataxia syndrome in a Turkish child," 17. International Child Neurology Congress, Antalya, Turkey, 2022

İNCECİK, FARUK Et Al. "Homozygous mutation in CWF19L1 with recessive ataxia syndrome in a Turkish child." 17. International Child Neurology Congress , Antalya, Turkey, 2022

İNCECİK, F. HERGÜNER, M. Ö. And TUĞ BOZDOĞAN, S. (2022) . "Homozygous mutation in CWF19L1 with recessive ataxia syndrome in a Turkish child." 17. International Child Neurology Congress , Antalya, Turkey.

@conferencepaper{conferencepaper, author={FARUK İNCECİK Et Al. }, title={Homozygous mutation in CWF19L1 with recessive ataxia syndrome in a Turkish child}, congress name={17. International Child Neurology Congress}, city={Antalya}, country={Turkey}, year={2022}}