A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families by Al‐Sulaiman, Reem, Othman, Amna, El‐Akouri, Karen, Fareed, Shehab, AlMulla, Hajer, Sukik, Aseel, Al‐Mureikhi, Mariam, Shahbeck, Noora, Ali, Rehab, Al‐Mesaifri, Fatma, Musa, Sara, Al‐Mulla, Mariam, Ibrahim, Khalid, Mohamed, Khalid, Al‐Nesef, Maryam Ali, Ehlayel, Mohammad, Ben‐Omran, Tawfeg

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