D. Tezen Et Al. , "Four Turkish families with hyperekplexia: A missense mutation and the exon 1–7 deletion in the GLRA1 gene," Parkinsonism and Related Disorders , vol.105, pp.128-131, 2022
Tezen, D. Et Al. 2022. Four Turkish families with hyperekplexia: A missense mutation and the exon 1–7 deletion in the GLRA1 gene. Parkinsonism and Related Disorders , vol.105 , 128-131.
Tezen, D., Şimşir, G., Çokar, Ö., Demirbilek, V., Başak, A. N., & Yapıcı, Z., (2022). Four Turkish families with hyperekplexia: A missense mutation and the exon 1–7 deletion in the GLRA1 gene. Parkinsonism and Related Disorders , vol.105, 128-131.
Tezen, Didem Et Al. "Four Turkish families with hyperekplexia: A missense mutation and the exon 1–7 deletion in the GLRA1 gene," Parkinsonism and Related Disorders , vol.105, 128-131, 2022
Tezen, Didem Et Al. "Four Turkish families with hyperekplexia: A missense mutation and the exon 1–7 deletion in the GLRA1 gene." Parkinsonism and Related Disorders , vol.105, pp.128-131, 2022
Tezen, D. Et Al. (2022) . "Four Turkish families with hyperekplexia: A missense mutation and the exon 1–7 deletion in the GLRA1 gene." Parkinsonism and Related Disorders , vol.105, pp.128-131.
@article{article, author={Didem Tezen Et Al. }, title={Four Turkish families with hyperekplexia: A missense mutation and the exon 1–7 deletion in the GLRA1 gene}, journal={Parkinsonism and Related Disorders}, year=2022, pages={128-131} }