Associated Papers
High-frequency actionable pathogenic exome variants in an average-risk cohort.
Rego S et al.
Cold Spring Harbor Molecular Case Studies, 2018
30487145 (PubMed )
Supplement: supp_mcs.a003178_Supplemental_File_3.xlsx › Sheet1
FOXG1 Mutation is a Low-Incidence Genetic Cause in Atypical Rett Syndrome.
Byun CK et al.
Child Neurology Open, 0
A case of congenital Rett variant in a Chinese patient caused by a FOXG1 mutation.
Niu Y et al.
Annals of Saudi Medicine, 0
Select a paper to view details