IndraLab

Statements


SCN1A activates FMH 1. 1 / 1
| 1

reach
"Approaches to identified genes for monogenic subtypes migraine (e.g. Familial Hemiplegic Migraine - FHM) has been successful (CACNA1A, ATP1A2, SCN1A genes causing FMH 1, 2 and 3 respectively) [XREF_BIBR - XREF_BIBR]."