Cite
HARVARD Citation
Janecke, A. et al. (2017). Deficiency of the sphingosine‐1‐phosphate lyase SGPL1 is associated with congenital nephrotic syndrome and congenital adrenal calcifications. Human mutation. 38 (4), pp. 365-372. [Online].
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Janecke, A. et al. (2017). Deficiency of the sphingosine‐1‐phosphate lyase SGPL1 is associated with congenital nephrotic syndrome and congenital adrenal calcifications. Human mutation. 38 (4), pp. 365-372. [Online].