Werner, K. M. Et Al. 2022. D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.188, no.1 , 357-363.

Werner, K. M., Cox, A. J., Qian, E., Jain, P., Ji, W., Tikhonova, I., ... Castaldi, C.(2022). D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.188, no.1, 357-363.

Werner, Kelly Et Al. "D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia," AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.188, no.1, 357-363, 2022

Werner, Kelly M. Et Al. "D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.188, no.1, pp.357-363, 2022

Werner, K. M. Et Al. (2022) . "D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.188, no.1, pp.357-363.

@article{article, author={Kelly M. Werner Et Al. }, title={D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia}, journal={AMERICAN JOURNAL OF MEDICAL GENETICS PART A}, year=2022, pages={357-363} }