Gene therapy for spinal muscular atrophy: the Qatari experience
Ali, Hossamaldein Gaber, Ibrahim, Khalid, Elsaid, Mahmoud Fawzi, Mohamed, Reem Babiker, Abeidah, Mahmoud I. A., Al Rawwas, Azhar Othman, Elshafey, Khaled, Almulla, Hajer, El-Akouri, Karen, Almulla, Mariam, Othman, Amna, Musa, Sara, Al-Mesaifri, Fatma, Ali, Rehab, Shahbeck, Noora, Al-Mureikhi, Mariam, Alsulaiman, Reem, Alkaabi, Saad, Ben-Omran, Tawfeg
Published in Gene therapy (01.11.2021)
Published in Gene therapy (01.11.2021)
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Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in DCAF17: Report of 58 additional patients from Qatar and literature review
Ali, Rehab, Al‐Dewik, Nader, Mohammed, Shayma, Elfituri, Mahmud, Agouba, Sahar, Musa, Sara, Mahmoud, Laila, Almulla, Mariam, El‐Akouri, Karen, Mohd, Howaida, Bux, Reem, Almulla, Hajer, Othman, Amna, Al‐Mesaifri, Fatma, Shahbeck, Noora, Al‐Muriekhi, Mariam, Khalifa, Amal, Al‐Sulaiman, Reem, Ben‐Omran, Tawfeg
Published in American journal of medical genetics. Part A (01.01.2022)
Published in American journal of medical genetics. Part A (01.01.2022)
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Journal Article
A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families
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
Published in American journal of medical genetics. Part A (01.11.2020)
Published in American journal of medical genetics. Part A (01.11.2020)
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Journal Article