Pehlivan, D. Et Al. 2015. Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis. HUMAN GENETICS , vol.134, no.6 , 671-673.

Pehlivan, D., Akdemir, Z. C., Karaca, E., Bayram, Y., Jhangiani, S., Yildiz, E. P., ... Muzny, D.(2015). Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis. HUMAN GENETICS , vol.134, no.6, 671-673.

Pehlivan, Davut Et Al. "Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis," HUMAN GENETICS , vol.134, no.6, 671-673, 2015

Pehlivan, Davut Et Al. "Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis." HUMAN GENETICS , vol.134, no.6, pp.671-673, 2015

Pehlivan, D. Et Al. (2015) . "Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis." HUMAN GENETICS , vol.134, no.6, pp.671-673.

@article{article, author={Davut Pehlivan Et Al. }, title={Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis}, journal={HUMAN GENETICS}, year=2015, pages={671-673} }