Suchergebnisse - (Person:"Veerapandiyan, Aravindhan")

PubPharm (2)

1

Variable penetrance of Andersen-Tawil syndrome in a family with a rare missense KCNJ2 mutation

enthalten in: Neurology. Genetics | 2018

von Deeb, R. | Veerapandiyan, A. | Tawil, R. | +1

2

Novel mutation in mitochondrial DNA in 2 siblings with Leigh syndrome

enthalten in: Neurology. Genetics | 2016

von Veerapandiyan, A. | Chaudhari, A. | Traba, C. | +1

1
[1]