A. B. Dirim Et Al. , "Late diagnosis of a rare multisystemic genetic disorder: Transaldolase deficiency due to homozygous TALDO1 c.345dupA variant," NEPHROLOGY , vol.29, no.1, pp.55-56, 2024
Dirim, A. B. Et Al. 2024. Late diagnosis of a rare multisystemic genetic disorder: Transaldolase deficiency due to homozygous TALDO1 c.345dupA variant. NEPHROLOGY , vol.29, no.1 , 55-56.
Dirim, A. B., Kalayci, T., Safak, S., Garayeva Guller, N., Oto, Ö. A., Artan, A. S., ... Ozturk, Ş.(2024). Late diagnosis of a rare multisystemic genetic disorder: Transaldolase deficiency due to homozygous TALDO1 c.345dupA variant. NEPHROLOGY , vol.29, no.1, 55-56.
Dirim, Ahmet Et Al. "Late diagnosis of a rare multisystemic genetic disorder: Transaldolase deficiency due to homozygous TALDO1 c.345dupA variant," NEPHROLOGY , vol.29, no.1, 55-56, 2024
Dirim, Ahmet B. Et Al. "Late diagnosis of a rare multisystemic genetic disorder: Transaldolase deficiency due to homozygous TALDO1 c.345dupA variant." NEPHROLOGY , vol.29, no.1, pp.55-56, 2024
Dirim, A. B. Et Al. (2024) . "Late diagnosis of a rare multisystemic genetic disorder: Transaldolase deficiency due to homozygous TALDO1 c.345dupA variant." NEPHROLOGY , vol.29, no.1, pp.55-56.
@article{article, author={Ahmet Burak DİRİM Et Al. }, title={Late diagnosis of a rare multisystemic genetic disorder: Transaldolase deficiency due to homozygous TALDO1 c.345dupA variant}, journal={NEPHROLOGY}, year=2024, pages={55-56} }