Huemer, M. Et Al. 2016. Clinical phenotype, biochemical profile, and treatment in 19 patients with arginase 1 deficiency. JOURNAL OF INHERITED METABOLIC DISEASE , vol.39, no.3 , 331-340.

Huemer, M., Carvalho, D. R., Brum, J. M., Unal, Ö., COŞKUN, T., Weisfeld-Adams, J. D., ... Schrager, N. L.(2016). Clinical phenotype, biochemical profile, and treatment in 19 patients with arginase 1 deficiency. JOURNAL OF INHERITED METABOLIC DISEASE , vol.39, no.3, 331-340.

Huemer, Martina Et Al. "Clinical phenotype, biochemical profile, and treatment in 19 patients with arginase 1 deficiency," JOURNAL OF INHERITED METABOLIC DISEASE , vol.39, no.3, 331-340, 2016

Huemer, Martina Et Al. "Clinical phenotype, biochemical profile, and treatment in 19 patients with arginase 1 deficiency." JOURNAL OF INHERITED METABOLIC DISEASE , vol.39, no.3, pp.331-340, 2016

Huemer, M. Et Al. (2016) . "Clinical phenotype, biochemical profile, and treatment in 19 patients with arginase 1 deficiency." JOURNAL OF INHERITED METABOLIC DISEASE , vol.39, no.3, pp.331-340.

@article{article, author={Martina Huemer Et Al. }, title={Clinical phenotype, biochemical profile, and treatment in 19 patients with arginase 1 deficiency}, journal={JOURNAL OF INHERITED METABOLIC DISEASE}, year=2016, pages={331-340} }