Associated Papers
Charcot-Marie-Tooth Disease Type 4H Resulting from Compound Heterozygous Mutations in FGD4 from Nonconsanguineous Korean Families.
Hyun YS et al.
Annals of Human Genetics, 2015
A novel mutation in FGD4/FRABIN causes Charcot Marie Tooth disease type 4H in patients from a consanguineous Tunisian family.
Boubaker C et al.
Annals of Human Genetics, 2013
Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4.
Stendel C et al.
American Journal of Human Genetics, 2007
Select a paper to view details