I. KARACAN Et Al. , "A novel ATP6V0A2 frameshift mutation causing autosomal recessive cutis laxa with bleeding diathesis and defective wound healing," ESHG 2016 , 2016
KARACAN, I. Et Al. 2016. A novel ATP6V0A2 frameshift mutation causing autosomal recessive cutis laxa with bleeding diathesis and defective wound healing. ESHG 2016 .
KARACAN, I., DİZ KÜÇÜKKAYA, R., TOLUN, A., HANÇER, V. S., & TAHİR TURANLI, E., (2016). A novel ATP6V0A2 frameshift mutation causing autosomal recessive cutis laxa with bleeding diathesis and defective wound healing . ESHG 2016
KARACAN, Ilker Et Al. "A novel ATP6V0A2 frameshift mutation causing autosomal recessive cutis laxa with bleeding diathesis and defective wound healing," ESHG 2016, 2016
KARACAN, Ilker Et Al. "A novel ATP6V0A2 frameshift mutation causing autosomal recessive cutis laxa with bleeding diathesis and defective wound healing." ESHG 2016 , 2016
KARACAN, I. Et Al. (2016) . "A novel ATP6V0A2 frameshift mutation causing autosomal recessive cutis laxa with bleeding diathesis and defective wound healing." ESHG 2016 .
@conferencepaper{conferencepaper, author={Ilker KARACAN Et Al. }, title={A novel ATP6V0A2 frameshift mutation causing autosomal recessive cutis laxa with bleeding diathesis and defective wound healing}, congress name={ESHG 2016}, city={}, country={}, year={2016}}