D. Gül Et Al. , "A novel homozygous frameshift SPTBN2 gene mutation associated with Spinocerebellar Ataxia-14," 13th BALKAN CONGRESS of HUMAN GENETİC , Edirne, Turkey, 2019
Gül, D. Et Al. 2019. A novel homozygous frameshift SPTBN2 gene mutation associated with Spinocerebellar Ataxia-14. 13th BALKAN CONGRESS of HUMAN GENETİC , (Edirne, Turkey).
Gül, D., Doğru, Z., Çaralan, E. F., Yüzel, Y., Dursun, Ş., SEYHAN, S., ... AYAZ, A.(2019). A novel homozygous frameshift SPTBN2 gene mutation associated with Spinocerebellar Ataxia-14 . 13th BALKAN CONGRESS of HUMAN GENETİC, Edirne, Turkey
Gül, Demet Et Al. "A novel homozygous frameshift SPTBN2 gene mutation associated with Spinocerebellar Ataxia-14," 13th BALKAN CONGRESS of HUMAN GENETİC, Edirne, Turkey, 2019
Gül, Demet Et Al. "A novel homozygous frameshift SPTBN2 gene mutation associated with Spinocerebellar Ataxia-14." 13th BALKAN CONGRESS of HUMAN GENETİC , Edirne, Turkey, 2019
Gül, D. Et Al. (2019) . "A novel homozygous frameshift SPTBN2 gene mutation associated with Spinocerebellar Ataxia-14." 13th BALKAN CONGRESS of HUMAN GENETİC , Edirne, Turkey.
@conferencepaper{conferencepaper, author={Demet Gül Et Al. }, title={A novel homozygous frameshift SPTBN2 gene mutation associated with Spinocerebellar Ataxia-14}, congress name={13th BALKAN CONGRESS of HUMAN GENETİC}, city={Edirne}, country={Turkey}, year={2019}}