Lehtokari, V. Et Al. 2008. Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.16, no.9 , 1055-1061.

Lehtokari, V., Pelin, K., Donner, K., Voit, T., Rudnik-Schoeneborn, S., Stoetter, M., ... TALİM, B.(2008). Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.16, no.9, 1055-1061.

Lehtokari, Vilma-Lotta Et Al. "Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.16, no.9, 1055-1061, 2008

Lehtokari, Vilma-Lotta Et Al. "Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.16, no.9, pp.1055-1061, 2008

Lehtokari, V. Et Al. (2008) . "Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.16, no.9, pp.1055-1061.

@article{article, author={Vilma-Lotta Lehtokari Et Al. }, title={Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2008, pages={1055-1061} }