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., GÜRAN, 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} }