CACNB2
Voltage-dependent L-type calcium channel subunit beta-2 is a protein that in humans is encoded by the CACNB2 gene.
Clinical significance
Mutation in the CACNB2 gene are associated with Brugada syndrome, autism, attention deficit-hyperactivity disorder (ADHD), bipolar disorder, major depressive disorder, and schizophrenia.
See also
References
Further reading
External links
This page contains text from Wikipedia, the Free Encyclopedia - https://wn.com/CACNB2
Podcasts:
PLAYLIST TIME: