MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutationHow to cite this article: Kalay E, Uzumcu A, Krieger E, Çaylan R, Uyguner O, Ulubil‐Emiroglu M, Erdol H, Kayserili H, Hafiz G, Başerer N, Heister AJGM, Hennies HC, Nürnberg P, Başaran S, Brunner HG, Cremers CWRJ, Karaguzel A, Wollnik B, Kremer H. 2007. MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation. Am J Med Genet Part A 143A:2382–2389.

Autor: Kalay, Ersan, Uzumcu, Abdullah, Krieger, Elmar, Çaylan, Refik, Uyguner, Oya, Ulubil‐Emiroglu, Melike, Erdol, Hidayet, Kayserili, Hülya, Hafiz, Gunter, Başerer, Nermin, Heister, Angelien J.G.M., Hennies, Hans C., Nürnberg, Peter, Başaran, Seher, Brunner, Han G., Cremers, Cor W.R.J., Karaguzel, Ahmet, Wollnik, Bernd, Kremer, Hannie

Publikováno v: American Journal of Medical Genetics. Part A; October 2007, Vol. 143 Issue: 20 p2382-2389, 8p

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