Cite
HARVARD Citation
Roifman, M. et al. (2020). Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiency. Clinical genetics. 98 (6), pp. 613-619. [Online].
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Roifman, M. et al. (2020). Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiency. Clinical genetics. 98 (6), pp. 613-619. [Online].