L. AKIN Et Al. , "A novel homozygous EIF2AK3 missense mutation in a patient with Wolcott-Rallison syndrome.," 51st Annual Meeting of the ESPE 2012 , vol.78, Germany, pp.158, 2012
AKIN, L. Et Al. 2012. A novel homozygous EIF2AK3 missense mutation in a patient with Wolcott-Rallison syndrome.. 51st Annual Meeting of the ESPE 2012 , (Germany), 158.
AKIN, L., KURTOĞLU, S., Flanagan, S. E., Kendirci, M., Htipoglu, N., Kapoor, R. R., ... Hussain, K.(2012). A novel homozygous EIF2AK3 missense mutation in a patient with Wolcott-Rallison syndrome. . 51st Annual Meeting of the ESPE 2012 (pp.158). , Germany
AKIN, Leyla Et Al. "A novel homozygous EIF2AK3 missense mutation in a patient with Wolcott-Rallison syndrome.," 51st Annual Meeting of the ESPE 2012, Germany, 2012
AKIN, Leyla Et Al. "A novel homozygous EIF2AK3 missense mutation in a patient with Wolcott-Rallison syndrome.." 51st Annual Meeting of the ESPE 2012 , Germany, pp.158, 2012
AKIN, L. Et Al. (2012) . "A novel homozygous EIF2AK3 missense mutation in a patient with Wolcott-Rallison syndrome.." 51st Annual Meeting of the ESPE 2012 , Germany, p.158.
@conferencepaper{conferencepaper, author={Leyla AKIN Et Al. }, title={A novel homozygous EIF2AK3 missense mutation in a patient with Wolcott-Rallison syndrome.}, congress name={51st Annual Meeting of the ESPE 2012}, city={}, country={Germany}, year={2012}, pages={158} }