| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 9377711 | Biological Psychiatry | 2005 | 7 Pages |
Abstract
Association of MLC1 with SCZ and BPAD suggests involvement of a common pathway. Rare missense mutations and common variants associated with BPAD favors hypothesis about likely involvement of both rare and common polymorphisms in etiology of this complex disorder.
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Authors
Ranjana Verma, Mitali Mukerji, Deepak Grover, Chandrika B-Rao, Swapan Kumar Das, Shobana Kubendran, Sanjeev Jain, Samir K. Brahmachari,