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HARVARD Citation
Khan, M. et al. (2021). Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family. Journal of gene medicine. p. n/a. [Online].
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Khan, M. et al. (2021). Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family. Journal of gene medicine. p. n/a. [Online].