TRPM6 mutation: A novel cause of "reversible" infantile epileptic encephalopathy
Neurol India
.
2016 Sep-Oct;64(5):1037-8.
doi: 10.4103/0028-3886.190253.
Authors
Minal Vikram Kekatpure
1
,
Saumil Gaur
2
,
Gopal Krishna Dash
3
,
Subramanian Kannan
4
Affiliations
1
Department of Neurology, Division of Pediatric Neurology, Narayana Health, Mazumdar Shaw Medical Center, Bengaluru, Karnataka, India.
2
Department of Pediatrics, Division of Pediatric Neurology, Narayana Health, Mazumdar Shaw Medical Center, Bengaluru, Karnataka, India.
3
Department of Neurology, Division of Epileptology, Narayana Health, Mazumdar Shaw Medical Center, Bengaluru, Karnataka, India.
4
Department of Endocrinology, Narayana Health, Mazumdar Shaw Medical Center, Bengaluru, Karnataka, India.
PMID:
27625251
DOI:
10.4103/0028-3886.190253
No abstract available
Publication types
Letter
MeSH terms
Brain Diseases / genetics*
Epilepsy / genetics*
Humans
Infant
Mutation
Spasms, Infantile / genetics*
TRPM Cation Channels / genetics*
Substances
TRPM Cation Channels
TRPM6 protein, human