Cite
HARVARD Citation
Lenz, D. et al. (2018). SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN). Genetics in medicine. pp. 1255-1265. [Online].
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Lenz, D. et al. (2018). SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN). Genetics in medicine. pp. 1255-1265. [Online].