Variable penetrance of Andersen-Tawil syndrome in a family with a rare missense KCNJ2 mutation
Deeb, Reem, Veerapandiyan, Aravindhan, Tawil, Rabi, Treidler, SimonaVolume:
4
Language:
english
Journal:
Neurology Genetics
DOI:
10.1212/NXG.0000000000000284
Date:
December, 2018
File:
PDF, 395 KB
english, 2018