Absence of GABRA1 Ala322Asp mutation in juvenile myoclonic epilepsy families from India

A. Kapoor, J. Vijai, H. M. Ravishankar, P. Satishchandra, K. Radhakrishnan, A. Anand

Research output: Contribution to journalArticlepeer-review

Fingerprint Dive into the research topics of 'Absence of GABRA1 Ala322Asp mutation in juvenile myoclonic epilepsy families from India'. Together they form a unique fingerprint.

Medicine & Life Sciences