Publication | Closed Access

A novel c.2T > C mutation of the KDM5C/JARID1C gene in one large family with X-linked intellectual disability

Genome InstabilityMendelian DisorderC MutationGenetic DisorderGeneticsLarge FamilyNovel C.2tMolecular BiologyMolecular GeneticsMedical GeneticsDisease Gene IdentificationMedicineClinical Genetics