Varaico: Literature-Extracted Genetic Variants

Gene:AR
Variant:p.P152R
Back to variants list

AR

NM_000044.6:p.P152R

Associated Papers

X chromosome inactivation in Rett Syndrome and its correlations with MECP2 mutations and phenotype.

Xinhua Bao et al.

Journal of Child Neurology, 2008

Influence of MECP2 gene mutation and X-chromosome inactivation on the Rett syndrome phenotype.

Chae JH et al.

Journal of Child Neurology, 2004

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."