Cite
HARVARD Citation
Hu, X. et al. (2022). PRKG1 mutation identified by whole-exome sequencing: a potential genetic etiology for He-Zhao deficiency. Journal of bio-X research. 5 (3), pp. 118-124. [Online].
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Hu, X. et al. (2022). PRKG1 mutation identified by whole-exome sequencing: a potential genetic etiology for He-Zhao deficiency. Journal of bio-X research. 5 (3), pp. 118-124. [Online].