Ucar, C. Et Al. 2021. A novel compound heterozygous mutation in the PYROXD1 gene in a patient with congenital myopathy. NEUROMUSCULAR DISORDERS , vol.31 .

Ucar, C., Yildirim, M., Bektas, O., Altintas, M., Sayar, Y., & Teber, S., (2021). A novel compound heterozygous mutation in the PYROXD1 gene in a patient with congenital myopathy. NEUROMUSCULAR DISORDERS , vol.31.

Ucar, C. Et Al. "A novel compound heterozygous mutation in the PYROXD1 gene in a patient with congenital myopathy," NEUROMUSCULAR DISORDERS , vol.31, 2021

Ucar, C. Et Al. "A novel compound heterozygous mutation in the PYROXD1 gene in a patient with congenital myopathy." NEUROMUSCULAR DISORDERS , vol.31, 2021

Ucar, C. Et Al. (2021) . "A novel compound heterozygous mutation in the PYROXD1 gene in a patient with congenital myopathy." NEUROMUSCULAR DISORDERS , vol.31.

@article{article, author={C. Ucar Et Al. }, title={A novel compound heterozygous mutation in the PYROXD1 gene in a patient with congenital myopathy}, journal={NEUROMUSCULAR DISORDERS}, year=2021}