NKX2.1 run-on mutation associated to familial brain-lung-thyroid syndrome.

Elena CavaliereAnna Jolanda GortanNadia PassonDora FabbroDario MarinMiryam CarecchioFederica BaldanSara Carmela CredendinoRosa GalloPaola CogoGiuseppe DamanteGabriella De Vita

Published in: Clinical genetics (2021)

Keyphrases

resting state
white matter
early onset
case report
functional connectivity
cerebral ischemia
multiple sclerosis