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Recently, mutations in several additional genes have been shown to cause SRPS: IFT80 [6,7] (MIM 611263), WDR35 [8,9] (MIM 614091), WDR19 [10] (MIM 614376), NEK1 [11,12] (MIM 263520), WDR34 [13,14] (MIM 615633), IFT140 [15,16] (MIM 266920), IFT172 [17] (MIM 615630), WDR60 [18] (MIM 615462), and TTC21B [19] (MIM 612014).
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