Identification of a rare novel kmt2c mutation that presents with schizophrenia in a multiplex family

Medicine and Dentistry

• Family 100%
• Lysine 33%
• Methyltransferase 33%
• Regulatory Mechanism 16%
• Analysis 16%
• Phenotype 16%
• Gene 16%
• Assay 16%
• Pathogenesis 16%
• Patient 16%
• Gene Expression 16%
• Syndrome 16%
• Brain 16%
• Missense Mutation 16%
• Neurodevelopmental Disorder 16%
• Epigenomics 16%
• Exome Sequencing 16%
• Histone H3 16%
• Genetic Disorder 16%
• Molecular Diagnosis 16%
• Dominant Inheritance 16%
• Genetic Counseling 16%
• Penetrance 16%

Neuroscience

• Dementia Praecox 100%
• Methyltransferase 28%
• Lysine 28%
• Gene 14%
• Phenotype 14%
• Intellectual Disability 14%
• Gene Expression 14%
• Epigenetics 14%
• Missense Mutation 14%
• Histone H3 14%
• Exome Sequencing 14%

Biochemistry, Genetics and Molecular Biology

• Mutation 100%
• Spectrum 18%
• Lysine 18%
• Gene Expression 9%
• Regulatory Mechanism 9%
• Nested Gene 9%
• Phenotype 9%
• Mental Retardation 9%
• Histone 9%
• Epigenetics 9%
• Genetic Disorder 9%
• Missense Mutation 9%
• Dominant Inheritance 9%
• Penetrance 9%
• Genetic Counseling 9%