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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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Al-Macki, Nabil.
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Journal articles
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(NBIA) Neurodegeneration with brain iron…
(1)
C19orf12 protein, Human
(1)
Genetics
(1)
Author
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Al-Macki, Nabil.
(1)
Rajab, Anna.
(2)
AbdulJabbar, Nemat AbdulRahman.
(1)
Abuelhassan, Abdelhameed A.
(1)
Adhikari, Swapan K.
(1)
Al-Amri, Mahmood Mohammed.
(1)
Al-Amriyah, Siham Sulaiman Saif
(1)
Al-Amriyah, Siham Sulaiman Saif.
(1)
AL-Azadjaliyah, .Asia Hassan
(1)
Al-Balushi, Said.
(1)
Al-Balushiyah, Zainab Mohammed Darwish.
(1)
Al-Bimaniyah, .Atika Ali
(1)
Al-Busaidiyah, .Aisha Khamis Amur
(1)
Al-Ghammariyah, Amjaad Saud.
(1)
Al-Hakmaniyah, Mariam Saleh Hamad.
(1)
Al-Harthy, .Salim Ali
(1)
Al-Hattaliyah, Hafidha Salim.
(1)
Al-Ibrahim, Nidal.
(1)
Al-Jaradi, Khalid Ali.
(1)
Al-Kasbiyah, Ghalia Mohammed.
(1)
Al-Kindiyah, Najma Mansoor Yahya.
(1)
Al-Kindiyah, Yusra Said Moosa.
(1)
Al-Lamkyah, .Ruwaida Naseer
(1)
Al-Mahruqiyah, Samira Hamed Mohamed.
(1)
Al-Musalhiyah, Khawla.
(1)
Al-Naabiyah, Farhat Mohamed Khalfan
(1)
Al-Naqbi, Ahmed Ibrahim.
(1)
Al-Reesyah, Iman Abdullah Humaid.
(1)
Al-Riyamiyah, Aisha Zahran Ahmed.
(1)
Al-Riyamiyah, Bashair Abdullah
(1)
Al-Saadiyah, Noura Daoud.
(1)
Al-Sharjyah, Nawal Khalfan.
(1)
Al-Shehhiyah, Halima.
(1)
Alafifi, Tariq.
(1)
Ba Awain, Salim Suhail Mohammed.
(1)
Bayoumi, Riad.
(1)
Berrazeg, M.
(1)
Dhar, Hansa.
(1)
Genchi, Francesco.
(1)
Hilles, Ayah Rebhi.
(1)
Jean, Mathilde.
(1)
Kiselev, Anton R.
(1)
Mahmood, Nailah.
(1)
Malla, Kalpana K.
(1)
Mozafarizadeh, Mina.
(1)
Mshelbwala, M.
(1)
Saad, Ashraf Abdullah.
(1)
Shalaby, Dalia.
(1)
Soltanpour, Mohammad Soleiman.
(1)
عيد, هالة فوزي محمد.
(1)
Publisher
Oman Medical Specialty Board
(1)
sfy39587stp18
