Cite
HARVARD Citation
Walber, S. et al. (2023). NGLY1 Deficiency: A Rare Genetic Disorder Unlocks Therapeutic Potential for Common Diseases. Israel journal of chemistry. 63 (1), p. n/a. [Online].
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Walber, S. et al. (2023). NGLY1 Deficiency: A Rare Genetic Disorder Unlocks Therapeutic Potential for Common Diseases. Israel journal of chemistry. 63 (1), p. n/a. [Online].