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Paper Details

A rare mutation of CACNA1C in a patient with bipolar disorder, and decreased gene expression associated with a bipolar-associated common SNP of CACNA1C in brain.
Mol Psychiatry
85
2014
BD, CACNA1C, CACNA1C SNP, CACNA1C SNP risk allele, CACNA1C gene, Cav1, TS, Timothy Syndrome, activated cells, autism, bipolar disorder, bipolar-associated common SNP, calcium, cardiac arrhythmias, cis-, cognitive impairment, developmental delays, excitable cells, expression quantitative trait locus, human, patient, patients, risk allele, rs1006737, single-nucleotide polymorphism, with BD i
Author NameAffiliation
Elliot S GershonUniversity of Chicago
Kay GrennanUniversity of Chicago
Judith A BadnerUniversity of Chicago
Ney Alliey-RodriguezUniversity of Chicago
Chunyu LiuUniversity of Illinois at Chicago, Central South University
Chunyu LiuUniversity of Illinois at Chicago, Central South University
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