G. Kayman Kürekçi Et Al. , "Desmin Mutation with an ultra rare and unique phenotype: Genome editing for a patient specific zebrafish model," keystone symposia Rare and Undiagnosed Diseases , Massachusetts, United States Of America, 2017
Kayman Kürekçi, G. Et Al. 2017. Desmin Mutation with an ultra rare and unique phenotype: Genome editing for a patient specific zebrafish model. keystone symposia Rare and Undiagnosed Diseases , (Massachusetts, United States Of America).
Kayman Kürekçi, G., Koyunlar, C., Kural Mangıt, E., Talim, B., Korkusuz, P., Erdem Özdamar, S., ... Puralı, N.(2017). Desmin Mutation with an ultra rare and unique phenotype: Genome editing for a patient specific zebrafish model . keystone symposia Rare and Undiagnosed Diseases, Massachusetts, United States Of America
Kayman Kürekçi, GÜLSÜM Et Al. "Desmin Mutation with an ultra rare and unique phenotype: Genome editing for a patient specific zebrafish model," keystone symposia Rare and Undiagnosed Diseases, Massachusetts, United States Of America, 2017
Kayman Kürekçi, GÜLSÜM K. Et Al. "Desmin Mutation with an ultra rare and unique phenotype: Genome editing for a patient specific zebrafish model." keystone symposia Rare and Undiagnosed Diseases , Massachusetts, United States Of America, 2017
Kayman Kürekçi, G. Et Al. (2017) . "Desmin Mutation with an ultra rare and unique phenotype: Genome editing for a patient specific zebrafish model." keystone symposia Rare and Undiagnosed Diseases , Massachusetts, United States Of America.
@conferencepaper{conferencepaper, author={GÜLSÜM KAYMAN KÜREKÇİ Et Al. }, title={Desmin Mutation with an ultra rare and unique phenotype: Genome editing for a patient specific zebrafish model}, congress name={keystone symposia Rare and Undiagnosed Diseases}, city={Massachusetts}, country={United States Of America}, year={2017}}