Khan M et al. Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family. J Gene Med. 2021;23(1):e3279. PMID: 32989887.
CC2D2A
Khan M et al. Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family. J Gene Med. 2021;23(1):e3279. PMID: 32989887.