FOXG1 - Forkhead box G1
|
|
Diseases list
- Disease-causing germline mutation(s) in Atypical Rett syndrome
- Role in the phenotype of 14q11.2 microduplication syndrome
- Role in the phenotype of 14q12 microdeletion syndrome
Assessed
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
