Novel mutation in forkhead box G1 (FOXG1) gene in an Indian patient with Rett syndrome.

Das, Dhanjit Kumar

Novel mutation in forkhead box G1 (FOXG1) gene in an Indian patient with Rett syndrome. [electronic resource] - Gene Mar 2014 - 109-12 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1879-0038

10.1016/j.gene.2013.12.063 doi


Amino Acid Sequence
Animals
Child
Female
Forkhead Transcription Factors--chemistry
Frameshift Mutation
Humans
India
Methyl-CpG-Binding Protein 2--genetics
Molecular Sequence Data
Nerve Tissue Proteins--chemistry
Protein Serine-Threonine Kinases--genetics
Rett Syndrome--diagnosis
Sequence Homology, Amino Acid