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Genetics
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Journal articles
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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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Genetics
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Brain neoplasms
(2)
Stroke
(2)
(NBIA) Neurodegeneration with brain iron…
(1)
Apolipoprotein E gene.
(1)
Apolipoproteins
(1)
Brain.
(1)
Brain Infarction
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Brain injuries--Oman
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Brain Ischemia
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Brain wounds and injuries
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Breast cancer--Oman
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C19orf12 protein, Human
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Cerebrovascular disease
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Cerebrovascular Disorders
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Diseases
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Heart diseases
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Magnetic Resonance Imaging.
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Nutrition surveys
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Nutrition surveys.
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Radiotherapy--Oman
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Tomography, X-Ray computed
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Al-Macki, Nabil.
(1)
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Oman Medical Specialty Board
(1)
sfy39587stp18
