S. Dedeoglu Et Al. , "Mutation identification and prediction for severe cardiomyopathy in Alström syndrome, and review of the literature for cardiomyopathy.," Orphanet journal of rare diseases , vol.17, no.1, pp.359, 2022
Dedeoglu, S. Et Al. 2022. Mutation identification and prediction for severe cardiomyopathy in Alström syndrome, and review of the literature for cardiomyopathy.. Orphanet journal of rare diseases , vol.17, no.1 , 359.
Dedeoglu, S., Dede, E., Oztunc, F., Gedikbasi, A., Yesil, G., & Dedeoglu, R., (2022). Mutation identification and prediction for severe cardiomyopathy in Alström syndrome, and review of the literature for cardiomyopathy.. Orphanet journal of rare diseases , vol.17, no.1, 359.
Dedeoglu, S Et Al. "Mutation identification and prediction for severe cardiomyopathy in Alström syndrome, and review of the literature for cardiomyopathy.," Orphanet journal of rare diseases , vol.17, no.1, 359, 2022
Dedeoglu, S Et Al. "Mutation identification and prediction for severe cardiomyopathy in Alström syndrome, and review of the literature for cardiomyopathy.." Orphanet journal of rare diseases , vol.17, no.1, pp.359, 2022
Dedeoglu, S. Et Al. (2022) . "Mutation identification and prediction for severe cardiomyopathy in Alström syndrome, and review of the literature for cardiomyopathy.." Orphanet journal of rare diseases , vol.17, no.1, p.359.
@article{article, author={S Dedeoglu Et Al. }, title={Mutation identification and prediction for severe cardiomyopathy in Alström syndrome, and review of the literature for cardiomyopathy.}, journal={Orphanet journal of rare diseases}, year=2022, pages={359} }