Article: TRPM6 mutation: A novel cause of "reversible" infantile epileptic encephalopathy.
2016 Volume 64, Issue 5, Page(s) 1037–1038
| MeSH term(s) | Brain Diseases/genetics ; Epilepsy/genetics ; Humans ; Infant ; Mutation ; Spasms, Infantile/genetics ; TRPM Cation Channels/genetics |
|---|---|
| Chemical Substances | TRPM Cation Channels ; TRPM6 protein, human |
| Language | English |
| Publishing date | 2016-09-14 |
| Publishing country | India |
| Document type | Letter |
| ZDB-ID | 415522-1 |
| ISSN | 1998-4022 ; 0028-3886 |
| ISSN (online) | 1998-4022 |
| ISSN | 0028-3886 |
| DOI | 10.4103/0028-3886.190253 |
| Database | MEDical Literature Analysis and Retrieval System OnLINE |
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