Publication | Open Access

The Xq22 Inversion Breakpoint Interrupted a Novel Ras-Like GTPase Gene in a Patient with Duchenne Muscular Dystrophy and Profound Mental Retardation

Mendelian DisorderGenetic DisorderDuchenne Muscular DystrophyGeneticsMedicineFragile X SpectrumXq22 Inversion BreakpointNeuroscienceDisease Gene IdentificationProfound Mental RetardationNeurogenetics