IndraLab

Statements


SCN8A activates mutated MATN3. 2 / 2
| 2

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"In this study, we explored the effect of Matn1 deletion on the phenotype of mice that were homozygous for a MED causing matrilin 3 mutation (Matn3 V194D)."

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"In conclusion, we explored the effect of matrilin 1 deletion in mice homozygous for a MED causing matrilin 3 mutation."