Approved symbol | MYRF |
---|---|
Approved name | myelin regulatory factor |
HGCN ID | HGNC:1181 |
Previous symbols | C11orf9 |
Inheritance | |
OMIM | 608329 |
Chromosome | 11q12.2 |
Panel(s) |
NGS Congenital Heart Defects NGS Mendeliome NGS White matter disease |