D. Pehlivan 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.671-3, 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 , 671-3.
Pehlivan, D., Akdemir, Z. C., Karaca, E., Bayram, Y., Jhangiani, S., Yildiz, E., ... 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, 671-3.
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, 671-3, 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.671-3, 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.671-3.
@article{article, author={Davut PEHLİVAN 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={671-3} }