4 results on '"Abubaker, Rayan"'
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2. A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
3. Novel variants causing megalencephalic leukodystrophy in Sudanese families
4. A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report
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