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Al-Macki, Nabil.
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A novel deletion mutation of exon 2 of the C19orf12 gene in an Omani family with mitochondrial membrane protein-associated neurodegeneration (MPAN).
Al-Macki, Nabil.
Oman Medical Specialty Board.
2017-01
A novel deletion mutation of exon 2 of the C19orf12 gene in an Omani family with mitochondrial membrane protein-associated neurodegeneration (MPAN).
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(NBIA) Neurodegeneration with brain iron…
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C19orf12 protein, Human
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Genetics
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Al-Macki, Nabil.
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, .Prashob PrasadPillay
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, .RashidKhan
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, Nawal KamisAl-Rasbyah
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.AL-Harthiyah, Tharaya Ahmed Saleh
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Al-Abri, Omar Said.
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Al-Akhzamiyah, Teeba Salim Hilal.
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Al-Alawiyah, Ruqaya Sulaiman.
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Al-Azaniyah, Mariam Abdullah Sulaiman.
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Al-Bzoor, Faten Maher Mohammed.
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Al-Habsiyah, Khoula Mubarak Amur.
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Al-Hinaiyah, Eiman Abdullah Mohammed
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Al-Kamalyah, Qater Al-Nada Abdullatif.
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Al-Kindiyah, Umaima Sulaiman Hamood.
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Al-Kindiyah, Umaima Suleiman Humood.
(1)
Al-Mazruiyah, Khoula Moosa Salem.
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Al-Rawas, Hana Bakhit Ali.
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Al-Saqry, Mohammed Ahmed Mohammed.
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Al-Yaqubiyah, Hekmat Shuwaired Said.
(1)
Al-Zaabi, Usama Abdullah Said.
(1)
Al Abdulqader, Zaher Hussein Ali.
(1)
Elmi, Alaa.
(1)
Gowda, S.
(1)
Grimm, Kirsten A.
(1)
Hummadi, Khalid Khazzal
(1)
Salama, T.
(1)
Verma, A.
(1)
Verma, Roshan Kumar.
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Waris, Muhammad Bilal.
(1)
Yule, Paul Alan.
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Oman Medical Specialty Board
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