Yavaş, C. Et Al. 2024. A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del). Genes and Genomics , vol.46, no.5 , 613-620.

Yavaş, C., Doğan, M., Eröz, R., & Türegün, K., (2024). A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del). Genes and Genomics , vol.46, no.5, 613-620.

Yavaş, Cüneyd Et Al. "A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del)," Genes and Genomics , vol.46, no.5, 613-620, 2024

Yavaş, Cüneyd Et Al. "A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del)." Genes and Genomics , vol.46, no.5, pp.613-620, 2024

Yavaş, C. Et Al. (2024) . "A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del)." Genes and Genomics , vol.46, no.5, pp.613-620.

@article{article, author={Cüneyd Yavaş Et Al. }, title={A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del)}, journal={Genes and Genomics}, year=2024, pages={613-620} }