Interstitial deletion of 3p22.3p22.2 encompassing ARPP21 and CLASP2 is a potential pathogenic factor for a syndromic form of intellectual disability: a co-morbidity model with additional copy number variations in a large family

Biochemistry, Genetics and Molecular Biology

• Nested Gene 100%
• Mental Retardation 100%
• Morbidity 100%
• Electric Potential 50%
• Phenotype 50%
• Candidate Gene 50%
• Copy-Number Variation 50%
• Association 50%
• Chromosome 3 50%