Varaico: Literature-Extracted Genetic Variants

Gene:MECP2
Variant:p.P184insFs
Back to variants list

MECP2

NM_001110792.2:p.P184insFs

Associated Papers

[FOXG1, a new gene responsible for the congenital form of Rett syndrome].

Roche-Martinez A et al.

Revista De Neurologia, 2011

Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.

Mencarelli MA et al.

Journal of Medical Genetics, 2010

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."