ArticleNeurogenetics2018
R106C TFG variant causes infantile neuroaxonal dystrophy "plus" syndrome.
A Catania et al.PubMed ↗Publisher ↗
No numbers read from the abstract.
9 papers cite it
this papercites it
ArticleNeurogenetics2018
A Catania et al.PubMed ↗Publisher ↗
No numbers read from the abstract.