A founderRAB27Avariant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families
- Resource Type
- Journal
- Authors
- 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
- Source
- AMERICAN JOURNAL OF MEDICAL GENETICS PART A; NOV 2020, 182 11, p2570-p2580, 11p.
- Subject
- Language
- English
- ISSN
- 15524833