Login / Signup

A founder mutation MLC1 c.736delA associated with megalencephalic leukoencephalopathy with subcortical cysts-1 in north Indian kindred.

S K VellarikkalR JayarajanA VermaR RaviV SenthilvelA KumarL SainiS GulatiM LalA MathurM K ChhetriMohammed FaruqVinod ScariaSridhar Sivasubbu
Published in: Clinical genetics (2018)
Keyphrases
  • white matter
  • tertiary care
  • multiple sclerosis