Publications
A novel homozygous SLC13A5 whole-gene deletion generated by Alu/Alu-mediated rearrangement in an Iraqi family with epileptic encephalopathy. Am J Med Genet A. 2021 ;185(7):1972-1980.
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Non-coding genetic variants in human disease. Hum Mol Genet. 2015 ;24(R1):R102-10.
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