Cite
HARVARD Citation
Abhyankar, A. et al. (2018). Clinical whole exome sequencing from dried blood spot identifies novel genetic defect underlying asparagine synthetase deficiency. Clinical case reports. 6 (1), pp. 200-205. [Online].
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Abhyankar, A. et al. (2018). Clinical whole exome sequencing from dried blood spot identifies novel genetic defect underlying asparagine synthetase deficiency. Clinical case reports. 6 (1), pp. 200-205. [Online].