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.
CC2D2ACC2D2AKhan 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.