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Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region

Mendelian DisorderGenetic DisorderGeneticsUnstable Genomic RegionNon-syndromic Mental RetardationFragile X SpectrumMolecular BiologyMolecular GeneticsDisease Gene IdentificationMedicine