M. WELZEL Et Al. , "Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1," EUROPEAN JOURNAL OF ENDOCRINOLOGY , vol.168, no.5, pp.707-715, 2013
WELZEL, M. Et Al. 2013. Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1. EUROPEAN JOURNAL OF ENDOCRINOLOGY , vol.168, no.5 , 707-715.
WELZEL, M., AKIN, L., BUESCHER, A., Guran, T., HAUFFA, B. P., Hoegler, W., ... LEONARDS, J.(2013). Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1. EUROPEAN JOURNAL OF ENDOCRINOLOGY , vol.168, no.5, 707-715.
WELZEL, Maik Et Al. "Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1," EUROPEAN JOURNAL OF ENDOCRINOLOGY , vol.168, no.5, 707-715, 2013
WELZEL, Maik Et Al. "Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1." EUROPEAN JOURNAL OF ENDOCRINOLOGY , vol.168, no.5, pp.707-715, 2013
WELZEL, M. Et Al. (2013) . "Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1." EUROPEAN JOURNAL OF ENDOCRINOLOGY , vol.168, no.5, pp.707-715.
@article{article, author={Maik WELZEL Et Al. }, title={Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1}, journal={EUROPEAN JOURNAL OF ENDOCRINOLOGY}, year=2013, pages={707-715} }